A Practical Guide To 3D Ultrasound
A Practical Guide To 3D Ultrasound
A Practical Guide To 3D Ultrasound
Reem S. Abu-Rustum
K21746
ISBN: 978-1-4822-1433-8
90000
9 781482 214338
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This book is dedicated to
All the “perfect imperfections”,
The fetuses scanned through the years…
and
To those through whom I came
And those who through me came
With eternal love and appreciation...
Contents
Foreword....................................................................................................................................................................................... ix
Preface.......................................................................................................................................................................................... xi
Chapter 6 3D Tools................................................................................................................................................................. 41
References................................................................................................................................................................................. 149
Index.......................................................................................................................................................................................... 157
vii
Foreword
Three-dimensional (3D) ultrasound was introduced to the This textbook, A Practical Guide to 3D Ultrasound,
medical community over 20 years ago when investigators created by Dr. Reem S. Abu-Rustum, helps fill this
in Europe and North America reported imaging fetal and important void. The chapters contain clear instructions
gynecological structures. In 2001 I purchased my first on how to image fetal as well as gynecological structures.
3D/4D ultrasound machine for clinical use and began an The beautiful images provided by the author are perhaps
exciting journey incorporating this technology into my the most compelling part of the textbook. The high quality
clinical practice. For the past 13 years 3D/4D technology of the images and the clarity of the instructions contained
has advanced to a point that it is indispensable for the serious within the text underscore the experience of Dr. Abu-Rustum
clinician who performs obstetrical, gynecological, and fetal in the 3D/4D ultrasound arena. This book will benefit both
echocardiographic examinations. the novice as well as the experienced physician/sonographer
As a result of this technology, there has been an explosion who uses 3D/4D technology in obstetrics and gynecological
of diagnostic tools, new terminology and concepts that have imaging.
required the practice of diagnostic ultrasound to be at a high Greggory R. DeVore, MD
level of commitment by the physician/sonographer providing Clinical Professor
ultrasound services to patients. While 3D/4D ultrasound is Department of Obstetrics and Gynecology
an exciting imaging modality, most of the medical literature David Geffen School of Medicine at UCLA
relating to this technology focuses on diagnostic results, Los Angeles, California, USA
with few articles addressing how to use the technology. A
comparison might be made when years ago travelers were Director of the Fetal Diagnostic Centers
told of the benefits of flying great distances by airplane, but Pasadena, Tarzana, and Lancaster, California, USA
did not understand that an experienced pilot was necessary
for this to be accomplished! Director of Perinatology
Providence Tarzana Medical Center
Tarzana, California, USA
ix
Preface
A Practical Guide to 3D Ultrasound was conceived with the This guide would not have been written had it not been for
beginner in volume sonography in mind. Having decided to the unconditional love and support of my lifelong motivator,
venture into this new world with added depth 10 years ago, I mentor and guide, my father Dr. Sameer Abu-Rustum, my
felt overwhelmed by all the terminology and the techniques mother Lina, my husband Kamil, my children Maria and
being used. Subsequently, I attended several courses and had Karim, and my sister Mira; they all believed in me and
the honor of visiting many labs examining all the basics in encouraged me over the years to persevere and complete this
order to decide what would be of utmost utility in my daily project despite many challenges.
clinical practice. As a result of this exposure to the experts, In addition, I wish to express my gratitude to Dr. Greggory
as well as a review of the clinically applicable literature, this DeVore for his invaluable guidance and constructive critique
guide was put forth. It is by no means comprehensive, but of this guide. Last but not least, I thank my editor, Mr. Robert
aims at summarizing all the basics in a concise and practical Peden, who saw the value of this project when I approached
manner, so that it can be used as an introduction to ease the him with my ambitious proposal; without his backing, this
transition into the third dimension. guide would not have been possible. I also thank Ms. Kate
I wish to acknowledge Drs. Amelia Cruz, Patrick Duff, Nardoni for all her meticulous work in putting this guide
and Douglas Richards, who first handed me the transducer, together.
and Dr. Kypros Nicolaides for sparking my interest in fetal May this guide maximize the utility of your volume
medicine. I also wish to recognize the tremendous impact sonography, enabling you to feel more secure in your
that the work of Drs. Alfred Abuhamad, Beryl Benacerraf, diagnostic capabilities and better able to reassure your
Bernard Benoit, Rabih Chaoui and Greggory DeVore has had patients as to the health of the future generations.
on my practice and on the birth of this guide; their pioneering
work has served as a constant source of inspiration over the Reem S. Abu-Rustum, MD
years. Center for Advanced Fetal Care
I am forever indebted to the wind that propelled me Tripoli, Lebanon
forward and the sun that lit my professional path, Dr. Keith
Stone.
S H’S 9 MONTHS
JOURNEY TO LIFE...
xi
1 Terminology and Basics
Introduction Z
Welcome to the world of volume sonography, a world with
added depth that enables you to obtain planes previously VOXEL = 3D
unattainable using conventional two-dimensional (2D) X
sonography. In volume sonography, the concept of the “voxel”
replaces the “pixel,” where you now have three intersect-
ing orthogonal or perpendicular planes with which you are
working—the X, Y, and Z planes (Figure 1.1). Where these
three planes intersect is the “reference dot,” an identifiable, Y
locatable point of interest that can be defined through its rela-
Y
tionship within the three planes. Within any acquired three-
dimensional (3D) volume is an infinite number of planes, PIXEL = 2D
stacked on top of each other, and containing within it all the
information needed to analyze that specific area or organ of
interest (Figure 1.2). For example, in the first trimester, a vol-
X
ume of the entire fetus may be obtained for analysis at any
subsequent point in the future (Abu-Rustum et al. 2012). This
volume, if obtained correctly, contains all the planes needed Figure 1.1 A cubic volume illustrating the three orthogonal
for a full evaluation of the first-trimester fetus (Figure 1.3). planes along the X, Y, and Z axes, representative of an acquired 3D
This also applies to a volume of the fetal heart that contains volume. At the bottom left-hand corner is a 2D rectangle along the
within it all the anatomic planes necessary for a complete X and Y axes, illustrating the 2D concept of a pixel. On the top right
assessment of the fetal heart and vessels (Abuhamad 2004). is a 3D rectangle along the X, Y, and Z axes, demonstrating the 3D
Once the volume of data is obtained and stored, it can subse- concept of a voxel.
quently be reformatted, post-processed, and displayed inter-
changeably in the multiplanar (Figure 1.4), surface-rendering
mode (Figure 1.5), or in any other mode at any given point Terminology
in the future.
With volume sonography, there is a new vocabulary to
learn (Table 1.1). Some of these terms are generic and oth-
Basic Concepts in the ers are specific to certain manufacturers. This is why one
Multiplanar Mode must become familiar with all the basic terms, their syn-
1. Marker dot: reference dot onyms, and their meanings. It then becomes intuitive as to
2. Address of the marker dot is determined by what is to be used where. The basic concept lies in obtain-
the intersection of the X, Y, Z axes (Figure 1.6) ing what is called a static volume and then visualizing it in
the three orthogonal planes in the multiplanar view. If it is
subsequently decided to manipulate the volume in order to
visualize the image using any of several display modes, this
The cornerstone of volume sonography is formed by three generates the rendered image. This can be surface mode
main concepts. These are addressed individually in the sub- (Figure 1.7), maximal mode (Figure 1.8), minimal mode
sequent chapters. (Figure 1.9), inversion mode (Figure 1.10), or any combina-
tion thereof, to name a few.
1
2 A Practical Guide to 3D Ultrasound
Designation for
the Cross Hairs
Figure 1.4 A 3D volume of a
20w6d fetal face displayed in the
three orthogonal planes. Note the
position of the reference dot (O). It is
the intersection of the cross-hairs in
each of the 3 planes.
Reference Dot
A C
Figure 1.6 A 3D volume of a 13w5d fetus. (A) This volume contains within it all the 2D anatomical planes necessary for a complete
assessment of the fetus. The reference dot, which is the intersection point of all three orthogonal planes, is placed on the fetal heart. It thus
localizes the fetal heart in all three orthogonal planes. (B) A 3D model illustrating the unique acquisition in the first trimester: it is possible
to obtain a volume of the entire fetus with a single 3D volume sweep. (C) A 3D model depicting the three intersecting orthogonal planes.
Table 1.1 Basic Terminology in Volume Sonography: Synonyms and Clinical Applicability
Key Word Synonym Clinical Applicability
3D Static 2D images, acquired together as part of For evaluating the surface or internal areas of interest
a volume and displayed in the three
orthogonal planes
4D Multiple volumes acquired per second Aids in visualizing fetal movement, facial grimaces, volume of a beating heart
and displayed to depict “3D in
motion”
CRI Compound resolution imaging Enhances the image resolution
Glass body Enhanced Doppler information in a Allows for vascular mapping and studies of vascular structures by minimizing the
gray-scale background gray-scale background and highlighting the vascular structure
HDlive 3D/4D technology with a virtual Gives a real surface-rendered image of the fetal face and outer surface; may also be
internal movable light source and used to visualize internal structures and can be combined with other 4D modalities
sophisticated skin-rendering
techniques
Inverse mode Inverts the gray-scale image where the Attenuates fluid-filled structures in the fetal brain, heart, gastrointestinal and
anechoic structures become genitourinary tracts, ovarian pathology, and any other fluid-filled areas
echogenic and vice versa
MagiCut Electronic scalpel with which to Allows volume editing in order to remove access areas and optimize visualization
sculpt through the volume of the area under study
Maximum mode x-ray mode Facilitates the study of all bony structures
Minimum mode Enhances Doppler information while Highlights the vascular tree and any fluid-filled, anechoic structures; best for
taking out all other gray-scale evaluation of the heart and fluid-filled structures
background information
OmniView The “any slice” technique Allows the slicing of any volume along any line, whether curvilinear or straight, to
display hard-to-obtain planes
Reference dot Marker dot, marker point The point of intersection of all three orthogonal planes through which rotation
along the three axes may be carried out
ROI Region of interest Allows the selection of an area of interest within the volume under study which
may be viewed in any of four directions
SonoAVC Automated volume calculator Allows the automatic selection of fluid-filled areas, color-codes them, and calculates
their volume; of maximal utility in ovarian follicular monitoring
SRI Speckle reduction imaging Refines the image by reducing the ultrasonographic speckle
STIC Spatiotemporal image correlation Enables obtaining and navigating through a volume of a beating heart, with or
without color Doppler, throughout one full cardiac cycle
Surface Image rendering of the fetal surface Surface topography to visualize the face and external structures; may also be
rendering utilized for the internal study of organs
TUI Tomographic ultrasound imaging A slicing technique, equivalent to CT, that generates multiple parallel slices, at a
user-set distance in mm, of the volume containing an area of interest, facilitating
the study of the spatial relationships between structures
VCAD Volume computer-aided diagnosis Automatic image retrieval of predefined standardized cardiac planes out of a
volume of the fetal heart which may allow a complete examination of the cardiac
structures out of the standardized volume
VCI-A and Volume contrast imaging Allows thick-slice scanning in order to decrease artifacts in either plane A or C;
VCI- C static VCI allows marked improvement in image quality
VOCAL Virtual organ computer-aided analysis Volume calculation of areas in question such as ovarian cysts, follicles, urine
production, lung mass, and so on, out of an acquired volume
6 A Practical Guide to 3D Ultrasound
IVC
Basic Causes of Artifacts
1. Motion of the fetus or mother
2. Rendering techniques
SVC
3. Shadowing artifacts
Reference
Dot
Artifacts may also raise the concern of the family and cause
DAo the inexperienced sonographer to overdiagnose (cleft lip) or
underdiagnose a certain condition if the area under exami-
Figure 1.9 A 3D volume of a 33-week fetus displayed in mini- nation is obscured. In addition, some of the most dangerous
mal mode. This volume utilizes color Doppler and depicts the aortic artifacts are generated as a result of the use of power and
arch (AoA) where the red reference dot is, descending aorta (DAo), color Doppler. For instance, when evaluating the ventricu-
as well as the right atrium (RA) with the superior and inferior venae lar septum, erroneous diagnosis of ventricular septal defects
cavae (SVC, IVC). may be made.
In gynecology, one of the most significant artifacts is the
Perhaps one of the greatest advantages of volume sonogra- echo enhancement artifact. This was described by Abuhamad
phy is the ability to standardize the examination of volumes, (2006) and is caused by the shadowing in the posterior myo-
defining spatial relationships between various anatomic metrium, whereby the myometrium now takes on the sono-
planes and organs, and enabling the automatic retrieval of graphic appearance of the endometrium. This artifact may
predefined planes of a specific area in question. This has occur when attempting to visualize the mid-coronal plane
been accomplished by Abuhamad et al. (2004, 2005, 2007) of the uterus, approaching it posterior to the myometrium.
with automation of the fetal heart, and the possible applica- If this volume is subsequently rendered in the multiplanar
tion of the same principles has been addressed in the first- mode, or when obtaining a thick slice, it may be erroneously
trimester fetus (Abu-Rustum et al. 2012). suggestive of a müllerian abnormality.
Practical Pearls
Figure 1.14 A 3D surface-rendered volume of a 22w3d fetus. In Figure 1.15 A 3D surface-rendered volume of a 21w5d fetus
this volume, rotation of the fetus has generated artifact suggestive using HDlive. In this volume, shadow artifact by the fetal hand
of a skull abnormality. Caution must be exercised in such cases to has resulted in an image that may raise concern for a facial cleft.
reassure the family as to the well-being of the fetus and to regener- With experience, the sonographer can anticipate such artifacts and
ate an artifact-free image of the fetal head. would exercise caution prior to generating such images so as to
avoid undue parental anxiety.
2 Volume Acquisition
Introduction Size of Box
The absolute determining factor for the quality of any 3D/4D The size of the box represents the entire area of interest. An
volume is the quality of the underlying 2D image and how example would be when acquiring a volume of the fetal heart
the actual volume was acquired. As such, one must have the at the level of the four-chamber view. The examiner needs
foresight as to what the volume is to be used for so that it is to decide how much of the chest is to be included around the
properly acquired in order to be able to generate adequate heart in order to set the acquisition box around that area of
images for evaluation. interest. This is exemplified in plane A, the reference plane,
in the multiplanar view (Figure 2.1).
Volume Acquisition This is determined by how much above and below the area
in question the volume should extend. For instance, when
As previously stated, the key to a good 3D volume is an acquiring a volume of the fetal heart at the level of the four-
underlying good 2D image and proper acquisition, keeping chamber view, is the plan to just include the heart or have
in mind the three basic keys to acquiring a volume: size of a volume that spans from the thyroid to the stomach? This
the box, angle of acquisition, and quality of acquisition. is exemplified in plane B, constructed from the 3D volume
9
10 A Practical Guide to 3D Ultrasound
data set in the multiplanar view (Figure 2.2). The angle Quality of Acquisition
depends on the type of transducer being used. In general, it
is double the distance that the probe moves on either side of The quality of acquisition determines its resolution. The higher
the reference plane. For instance, if the angle chosen is 30 the quality, the longer it takes to acquire the volume, thus there
degrees for the fetal heart, then the probe would acquire 15 is more chance for fetal movement and a greater probability
degrees on either side of (above and below) the four-cham- of artifacts. Keep in mind that a higher quality is required for
ber view, for a total of 30 degrees. Plane C is the third plane, the evaluation of internal structures, whereas a lower quality is
perpendicular to A and B and reconstructed from the vol- sufficient for the evaluation of the external surface. This does
ume data set. not hold true in areas without motion artifact, such as when
acquiring a volume of the uterus in gynecology where you
can use the widest angle and the largest box with the highest
resolution with minimal artifacts generated. Tables 2.1 and 2.2
cover the basic steps for volume acquisition.
A B
Table 2.1 Steps to Acquiring a Volume of the Fetal Heart and Chest
Step 1: Obtain the plane of the four-chamber view after having optimized your basic 2D settings (Figure 2.1)
Step 2: Select an angle of acquisition of 30 degrees a; this volume should subsequently span from the fetal stomach to the thyroid for a second-
trimester fetus
Step 3: Set the quality of the acquisition of the volume to “high” in the absence of fetal motion, and to “medium” in case of fetal motion
Step 4: Hit “freeze” as this should automatically sweep through the fetal chest, spanning 15 degrees above and below the four-chamber view in order
to acquire the volume and display it in the multiplanar mode along the three orthogonal planes
Step 5: Check plane A to make sure this displays the initially acquired reference plane (Figure 2.2)
Step 6: Check plane B to make sure it spans from the fetal stomach to the thyroid (Figure 2.2)
Step 7: Save the volume if it is adequate for later manipulation and offline analysis
a The degree of the sweep is related to gestational age. For example, 20 degrees at 20 weeks of gestation, 30 degrees at 30 weeks of gestation.
Figure 2.3 Face acquisition. (A) In order to acquire a 3D volume of the fetal face, optimize your 2D settings, and place the box of
acquisition around the fetal face while attempting to capture the image with a good amniotic fluid interphase in front of the fetal face.
The angle of acquisition is then selected, 65 degrees in this example, and the quality of the volume is then set. The volume is subsequently
acquired and saved. (B) A 3D model showing the plane of acquisition commencing with the fetal profile.
Figure 2.4 Once the volume is acquired it may be displayed in the multiplanar mode and surface rendering. Note the position of the box
of acquisition in plane A. The depth, represented by the angle of acquisition, is depicted in plane B and encompasses the entire width of the
face extending beyond each of the two orbits. The angle of acquisition can be seen in the top right-hand corner (underlined) as mid 2. In
addition, the quality of the volume is mid 2 (dashed underline).
12 A Practical Guide to 3D Ultrasound
This chapter focuses on volume manipulation so that the user The reference dot is the intersection point between all three
can optimize the image planes for display of the multiplanar orthogonal planes. Volume manipulation is facilitated by
(Figure 3.1) and render formats (Figures 3.2 and 3.3). placing the reference dot at a specific point within the vol-
ume. This subsequently becomes the pivotal point around
which the volume may be rotated along any of the three axes,
Volume Manipulation without losing its position, as it remains displayed in all three
orthogonal planes. The reference dot can be moved around so
After the volume is acquired, it is possible to manipulate and that it is set at a particular point of interest within the volume,
navigate through the volume utilizing the most appropriate and it can be seen in all three orthogonal planes simultane-
technique for a complete assessment of the area of interest. ously if the multiplanar mode is selected (Figure 3.4). For
This may be accomplished utilizing rotation through the ref- instance, if a volume of the fetal abdomen is obtained with
erence dot along the three axes. The volume may be manipu- the primary focus on the fetal stomach, then the reference
lated further by changing the size and direction from which dot can be placed on the fetal stomach and it is subsequently
the region of interest is examined. identified in all three orthogonal planes (Figure 3.5). In the
volume of the fetal abdomen, one would not lose the stomach,
if it is the focal point of interest, and any manipulation within
Basic Concepts for Volume that volume will occur around the stomach where it remains
Manipulation clearly displayed at all times and in all three orthogonal or
1. Placing the reference dot on the target area perpendicular planes, as the primary designated structure. If
within the volume tomographic ultrasound imaging (TUI) were to be utilized,
2. Rotating along the X, Y, and Z axes through the then the reference dot would locate the stomach in each of
reference dot the planes displayed (Figure 3.6). If the aorta becomes the
3. Selecting the size and direction from which to primary point of interest, then the reference point may be
view the region of interest moved from the stomach to the aorta for navigation within
the volume, with the aorta as the pivotal point (Figure 3.7).
Reference Dot
13
14 A Practical Guide to 3D Ultrasound
Figure 3.2 The same volume from Figure 3.1 displayed using surface rendering. In this case, the sonographer may also select to display
the volume in only one pane so that the rendered image will be the only image displayed without showing the images in planes A, B, and C.
Figure 3.3 A 3D volume of a 22w4d fetal chest displayed using the skeleton mode,
also known as maximum mode, clearly depicting the rib cage and all 12 ribs. Here the
single-pane view has been selected.
Volume Manipulation 15
Reference Dot
Figure 3.4 A transvaginal 3D volume of a multicystic ovary displayed in the three orthogonal planes
with the reference dot clearly visible in planes A, B, and C.
Reference Dot
Figure 3.5 A 3D volume of the abdomen of a 22w1d fetus acquired with an angle of 55 degrees and a
quality of high 2 (information in the top right-hand side of the image) displayed in the multiplanar mode.
The reference dot is placed in the fetal stomach, localizing it in each of the three planes.
16 A Practical Guide to 3D Ultrasound
Figure 3.6 The same 3D volume obtained for Figure 3.5 is now displayed using TUI with a slice thick-
ness of 2 mm. The reference dot remains in the stomach in all the planes. This becomes most useful in
determining spatial relationships between organs, or when evaluating the boundaries of a tumor.
Figure 3.7 The same 3D volume obtained for Figures 3.5 and 3.6 is still displayed using TUI with a
slice thickness of 2 mm; however, now the reference dot is moved to the aorta and it localizes the aorta in
all eight panes.
Volume Manipulation 17
To further navigate within the volume, rotation can be accom- It is also possible to scroll through the volume moving cepha-
plished along any of the three orthogonal planes (the X, Y, and lad or caudad. This can be carried out in any of the three
Z axes), with the reference dot as the point around which the orthogonal planes. For example, in the volume of a first-tri-
rotation occurs. Rotation along the X axis is accomplished mester fetus, this may be accomplished by moving the refer-
as if rotating in a ‘rotisserie’ mode (Figure 3.8). Rotation ence dot in plane A cephalad to reach the fetal head in plane
along the Y axis is in the orientation of the motion of a ‘drill’ B (Figure 3.11), or caudad to reach the fetal abdomen in plane
(Figure 3.9). Rotation along the Z axis is in a clockwise/coun- B (Figure 3.12). This may also be accomplished using the
terclockwise fashion within the image through the reference ‘depth’ button on the machine.
dot, in a ‘rocking’ motion (Figure 3.10).
A
X
Figure 3.8 3D volume of a 12w6d fetus displayed in the multiplanar mode. (A) The initial volume. (B) The volume after it has been
rotated along the X axis through the reference dot in the fetal neck in reference plane A as if rotated around a rotisserie. (C) 3D model depict-
ing X rotation.
18 A Practical Guide to 3D Ultrasound
Z
C
Figure 3.9 3D volume of a 12w6d fetus displayed in the multiplanar mode. (A) Initial volume. (B) Volume after it has been rotated along
the Y axis through the reference dot in the fetal neck in reference plane A as if rotated along the rotational axis of a drill. (C) 3D model
depicting Y rotation.
C Z
Figure 3.10 3D volume of a 12w6d fetus displayed in the multiplanar mode. (A) Initial volume. (B) Volume after it has been rotated
along the Z axis through the reference dot in the fetal neck in reference plane A as if in a rocking motion. (C) 3D model depicting Z rotation.
Volume Manipulation 19
Reference Dot
Reference Dot
B B
Figure 3.11 3D volume of a 12w6d fetus displayed in the Figure 3.12 3D volume of a 12w6d fetus displayed in the
multiplanar mode. (A) Initial volume with the reference dot at the multiplanar mode. (A) Initial volume with the reference dot at the level
level of the fetal neck in plane A generating an axial image of the of the fetal neck in plane A generating an axial image of the neck in
neck in plane B. (B) Volume after the reference dot in plane A has plane B. (B) Volume after the reference dot in plane A has been moved
been moved cephalad to the fetal head generating a new image in caudad to the fetal abdomen generating a new image in plane B of the
plane B of the fetal cranium. fetal abdominal circumference plane with a visible fetal stomach.
Stomach
Limb
A B
Figure 3.16 This is the same 3D volume of Figure 3.13. (A) The region of interest encompasses the entire abdomen with the direction
of view top to bottom starting outside the fetal skin as depicted by the line in plane A. This is depicted in the final rendered image where
a fetal limb is seen. (B) The size of the region of interest is changed and now the green viewing line starts at the level of the fetal stomach,
which can be seen in the final rendered image.
Stomach
22 A Practical Guide to 3D Ultrasound
Reference Dot
X DAo AoA
Figure 3.18 This is the same volume as in Figure 3.17. “Spinning” along the Y axis is carried out, resulting in complete visualization of
the aortic arch (AoA), head and neck vessels (*), and the descending aorta (DAo)
DA
Reference Dot DA
SVC
RA
Table 3.1 Steps in the Spin Technique Displaying the Outflow Tracts Out of a Volume of the Fetal Chest
Step 1: Select the 4 chamber view as your reference plane with the ultrasound beam perpendicular to the ventricular septum (Figure 3.17)
Step 2: Obtain a 3D sweep with an angle of acquisition of 30 degrees and a mid to high quality for the volume
Step 4: Place the reference point along the crux of the heart (Figure 3.17)
Step 5: Rotate the volume along the Y axis to depict the aortic arch along its entire length (Figure 3.18)
Step 6: Go back to the initial volume and scroll cephalad to the 3-vessel view and place the reference dot on the ductus arteriosus (Figure 3.19)
Step 7: Rotate along the Y axis to depict the ductal arch (Figure 3.20)
Step 8: Go back to the 3-vessel view and place the reference dot in the superior vena cava (Figure 3.21)
Step 9: Rotate along the Y axis to depict the bicaval view with the superior and inferior venae cavae visible entering the right atrium (Figure 3.22)
25
26 A Practical Guide to 3D Ultrasound
Figure 4.2 A 3D volume of the fetal face at 21w6d displayed using HDlive, a
new surface-rendering mode with an adjustable internal light source.
Table 4.1 Steps in Altering the ROI Orientation while Viewing the AV Valves
Step 1: Select the four-chamber view as your reference plane with the ultrasound beam parallel to the ventricular septum
Step 2: Obtain a 3D sweep with an angle of acquisition of 15 degrees and a mid to high quality for the volume
Step 3: Place the render box over the AV valves with the ROI orientation from the basal (atrial) side
Step 4: The AV valves are now depicted in the rendered image (Figure 4.3)
Step 5: Change the ROI orientation now to the apical (ventricular side) (Figure 4.4)
Step 6: The leaflets of the AV valves may now be visualized from the ventricular side in the final rendered image
The rendered image may be displayed in the surface skin-rendering techniques to generate lifelike images. The
mode (default setting on most machines); dynamic render- sonographer must keep in mind that for optimal results, it is
ing; or HDlive (Figure 4.7), which utilizes sophisticated necessary to remove any cord, placenta, or extremities by the
electronic scalpel (MagiCut) and to optimize the image prior
to activating HDlive. A unique feature of HDlive is the avail-
Basic Concepts in Obtaining ability of a movable internal light source that may be adjusted
a Surface-Rendered Image for optimal image display (Figure 4.8).
of the Fetal Face
1. A fluid–tissue interphase is required for opti- Maximum Mode
mal rendering of the image
2. Avoid obtaining a volume with the fetal cord The maximum mode is utilized to display the fetal skeleton
or an extremity covering the face – the ribs, spine, extremities, bony face, sutures of the fetal
3. To visualize the fetus face en face, start with skull, or cranium. The same basic principles of volume acqui-
the fetal profile (sagittal view) as the reference sition discussed in Chapter 2 apply here with respect to vol-
plane ume acquisition and the need to optimize the basic 2D image.
4. To visualize the fetal profile, start with an en However, when choosing the “render” mode, the maximum
face reference plane (coronal view) of the fetal mode is selected and the region of interest is selected around
face the area in question (Figure 4.9).
Volume Display 29
1 S
12
Figure 4.9 A 3D volume of a 21w4d fetus displayed in the skel-
etal (maximum) mode. Note that this mode highlights the bony
structures and enables visualizing the clavicles (C), scapula (S) as
well as all 12 ribs (1–12).
Whenever vascular or fluid-filled structures such as fetal ves- the vasculature of the Circle of Willis, where color Doppler
sels, heart, stomach, kidneys, or bladder are under exami- is also employed (Figure 4.10). In addition, high-definition
nation, the minimum mode may be utilized. The minimum flow and B flow may be utilized instead of color Doppler to
mode optimizes the parameters for visualizing the echo- further evaluate the area under study. The glass body mode
lucent areas. For example, if the Circle of Willis is to be is a compromise between minimum mode and regular imag-
evaluated, the 2D and color Doppler image settings should ing, where the gray scale is minimized but not completely
be optimized and the Circle of Willis should be the start- removed. This aids in maintaining the volume orientation of
ing reference plane when acquiring the volume. A 3D sweep the vasculature within the anatomical structures being stud-
may then be obtained, and the minimum mode is selected ied (Figure 4.11).
in order to remove all the gray-scale areas and to highlight
30 A Practical Guide to 3D Ultrasound
Inversion Mode of the area in question. An example of the utility of the inver-
sion mode is in evaluating a multicystic ovary (Figure 4.12).
The inversion mode is usually complementary to the mini- In addition, the inversion mode is useful for rendering a cast
mum mode, where the echolucent area under study in the of the area in question; for instance a ventricular septal defect
minimum mode may be “inverted” so that the gray scale (VSD) (Figure 4.13). A stepwise approach to inverting a vol-
is minimized and echolucent structures become echogenic, ume is described in Table 4.2.
further facilitating characterization and volume calculation
H&N
AoA
V
Figure 4.11 A sagittal 3D volume of a 22w6d fetus with color
C Doppler displayed using glass body mode. Here the gray scale is
minimized and the fetal vasculature is highlighted. In this case,
the aortic arch (AoA), with the head and neck vessels (H & N),
descending aorta (DAo) as well as the inferior vena cava (IVC)
are seen.
Volume Display 31
A B
C D
Figure 4.12 A transvaginal 3D volume of a multicystic ovary rendered using inversion mode. (A) Multiplanar display using VCI at a
slice thickness of 2 mm. (B) The volume is rendered using inversion mode. (C) The direction of the region of interest is changed to “top
to bottom” in reference plane A. (D) MagiCut as well as manipulation of the threshold, transparency and color are carried out for optimal
results for visualizing the cysts.
HD FB
Cl
H
S
LL
B
B
A
Figure 4.14 Tomographic ultrasound imaging (TUI). (A) A 3D volume of a 12w5d fetus displayed using TUI with an interslice distance
of 6 mm and VCI at a slice thickness of 2 mm. The planes depicting the head (HD), facial bones (FB), heart (H), stomach (S), cord insertion
(CI), bladder (B), and lower limbs (LL) are generated out of the volume. (B) A 3D model depicting the axial slicing of TUI.
5 Spatiotemporal Image Correlation
Reference Dot
33
34 A Practical Guide to 3D Ultrasound
The uniqueness of this technique is that the fetal heart can manufacturers have made it possible to carry out the off-line
be examined off-line, throughout a full cardiac cycle, dur- M-mode analysis on a STIC volume, and it is possible to
ing systole (Figure 5.3) and diastole (Figure 5.4), allowing a change the orientation of the M-line (Figure 5.7). It is also
complete and thorough evaluation of both structure and func- possible to invert a STIC volume (Figure 5.8) and to add it
tion. Navigating through a STIC volume enables the study to any of the color modes—color Doppler, power Doppler,
of wall motion (the study of atrioventricular and semilunar or high-definition flow – to further study the valves and the
valves in systole and diastole) (Figures 5.5 and 5.6). Certain vasculature in motion.
RV
LV
VS
VS
RV
RV
LV
LV
A B
Figure 5.7 The same STIC volume displayed using M-mode. (A) Orientation for the M-mode display
starts with the right ventricle (RV), the ventricular septum (VS), then the left ventricle (LV). (B) M-line is
rotated off-line 180 degrees, whereby the orientation for the M-mode display now becomes reversed start-
ing with the LV, VS, then RV.
VS
A B
Figure 5.8 A STIC volume of a 25w4d fetal heart rendered using inversion mode. (A) Multiplanar
display with render using inversion mode. (B) Single pane displayed of a rotated final-rendered volume.
This generates a cast of the heart showing the shape of the atria, the ventricles, and the symmetry. Note the
intact ventricular septum (VS). When the cineloop is activated the function may also be assessed.
A main limitation of this technique is the resolution in the in much loss of resolution. In addition, TUI may be employed
B and C planes (Figures 5.1, 5.2, 5.5, and 5.6). If the ulti- to retrieve all the respective anatomical planes out of the vol-
mate goal is the sagittal examination of the aortic and sag- ume (Figure 5.9) (DeVore et al. 2004). Table 5.1 covers the
ittal arches or the right atrial inflow, the volume should be basic steps for inverting a STIC volume of the fetal heart,
acquired in the sagittal plane and not constructed from the which may be visualized in a multitude of ways, including a
four-chamber view, because the reconstruction would result 3D cineloop (Figures 5.10–5.15).
Table 5.1 Steps to Obtaining and Inverting a STIC of the Fetal Heart
Step 1: Select the four-chamber view as your reference plane with the ultrasound beam parallel to the ventricular septum
Step 2: Obtain a 4D sweep with the acquisition box placed just around the heart, with an angle of acquisition of 15 to 30 degrees and a mid to
high quality for the volume
Step 3: Acquire the volume with color Doppler; the STIC volume is now displayed in the multiplanar mode in the three orthogonal planes as
cineloops of the beating heart (Figure 5.10)
Step 4: Render the volume with the direction of the region of interest as a back-to-front direction (Figure 5.11)
Step 5: Select inversion mode to invert the STIC volume and obtain a 4D inverted cast of the fetal heart; with the current settings, there will be
no clear cast (Figure 5.12)
Step 6: Adjust the threshold to roughly 120 and the mix to 100/0 to optimize the final rendered image (Figure 5.13)
Step 7: Select the single-image mode and rotate the volume along the three orthogonal planes and use MagiCut to remove the obscuring areas
(Figure 5.14)
Step 8: The final rendered inverted version of the fetal heart may now be displayed as a 2D image in any color (Figure 5.15) or it seen as a
cineloop of the beating heart
Spatiotemporal Image Correlation 37
DV SVC
A
Az o
A HN Az
DAo
RA
IVC
A B
Figure 5.9 STIC volume of the heart of a 23w4d fetus with high-definition flow is acquired at an angle of 20 degrees starting from
the sagittal plane. (A) Volume is displayed in the multiplanar mode. (B) Volume is displayed using TUI at a 2 mm interslice distance
automatically generating all the required anatomical sagittal planes out of the single STIC volume. Note the aortic arch (AoA) descending
aorta (DAo), head and neck vessels (HN), ductus venosus (DV), hypoechogenic azygous vein (Az) (no color uptake), right atrium (RA), and
superior and inferior venae cavae (SVC and IVC).
A C
Figure 5.10 STIC acquisition. (A) STIC volume with high-definition flow of a 21w5d heart is acquired at an angle of 20 degrees. It is
displayed in the multiplanar mode. (B) 3D model depicting the level of acquisition. (C) 3D model depicting the multiple overlaid 2D images.
For a STIC, the volume would be limited to the heart.
38 A Practical Guide to 3D Ultrasound
Figure 5.11 The same volume from Figure 5.11 is now rendered using surface rendering with the direction
of the region of interest set at a back-to-front direction.
Figure 5.12 Render mode now changed to inversion. However, at the current settings no image is generated.
Spatiotemporal Image Correlation 39
Figure 5.13 Mix and threshold settings are now adjusted, generating a cast of the fetal heart with the atrial
and ventricular septae visible
A B C
Figure 5.15 Postmanipulation. (A,B,C) Volume is now rotated along the three axes, and MagiCut is utilized to crop away any obscuring
areas. Volume is displayed in various color settings. It may be viewed as a cineloop and rotated along any of the three axes. Care must be
employed to not erroneously diagnose ventricular septal defects in this case, as these are rendering artifacts.
MagiCut
Volume Contrast Imaging
The electronic scalpel, MagiCut, is one of the most useful
tools, allowing the sonologist to sculpt away and remove any There are several slicing modalities that can be utilized for
structures that may be obscuring the area of interest. To use volume rendering in order to improve the visualization of
the MagiCut properly, the examiner must be aware of which the final rendered structure. One example is volume contrast
structures within the volume are to be evaluated and which imaging (VCI). This is a thick-slice technique where, instead
structures need to be removed. For optimal images, the vol- of a thin 2D image display, a thick slice along an adjust-
ume can be rotated along the three axes to ascertain the depth able thickness may be obtained, minimizing artifacts and
and direction of the structures that need to be removed using improving the quality of the image. VCI may be combined
41
42 A Practical Guide to 3D Ultrasound
OmniView
Figure 6.3 The volume is rotated along the Y axis and Figure 6.4 This is the final volume after completing MagiCut.
MagiCut is activated. MagiCut in this case employs “line Further anticlockwise rotation is carried out along the Y axis.
trace” to remove areas “within” the line. The excess placen- Finally, surface rendering is changed to HDlive, and the threshold
tal and other tissue is selected and removed. and light source are adjusted to generate this image. Note the ori-
entation of the light source depicted in the schematic at the bottom
right-hand corner of the image (*).
CB
Figure 6.5 A 3D
volume of the fetal brain
at 22w0d is displayed
using TUI at an interslice
Th
thickness of 2 mm. Note
where the interslice
thickness is designated
(*). The posterior fossa
with the cerebellum
(CB), thalami (Th),
posterior horn of the F CSP
lateral ventricle (Vp), falx
cerebri (F), and cavum
septi pellucidi (CSP) are
Vp
seen.
44 A Practical Guide to 3D Ultrasound
*
CB
Figure 6.6 The same
3D volume of Figure 6.5
now displayed using VCI
with a slice thickness of 2
Th
mm (seen at the top right-
hand corner [*]). The
posterior fossa with the
cerebellum (CB), thalami
(Th), posterior horn of the
lateral ventricle (Vp), falx
F CSP cerebri (F), and cavum
septi pellucidi (CSP) are
seen. Note the improve-
Vp
ment in the resolution and
definition of the image.
CC
L R
DAo
Ao
RL
LL
S
D
Figure 6.8 A 3D volume of a 21w5d fetal chest is obtained. The OmniView algorithm is employed with VCI at a slice thickness of 1 mm
utilizing three color-coded polylines. The first line (1) is drawn from the left (L) to the right (R) of the chest across both lungs, transecting
the aorta (Ao) in plane A. It generates an image of the descending aorta (DAo) in plane B. Line (2) is drawn from the posterior aspect of
the right lung to the anterior abdominal wall, generating an image of the right lung (RL) with a clear diaphragm (D) seen in plane D. Line
(3) is drawn from the posterior aspect of the left lung to the anterior abdominal wall, generating an image of the left lung (LL) with a clear
diaphragm (D), and the stomach (S), seen in plane C.
Figure 6.9 A 3D volume of the fetal chest and abdomen is obtained and
displayed in the coronal plane utilizing VCI at a slice thickness of 2.5 mm.
46 A Practical Guide to 3D Ultrasound
A C
Volume Computer-Aided Diagnosis navigation within the volume. The applicability of these vari-
ous tools is discussed further in the organ-specific chapters.
Volume computer-aided diagnosis (VCAD) is based on two
main concepts, as described by Abuhamad (2004). The first
concept states that any acquired volume contains within it all Practical Pearls
the 2D anatomical planes necessary for a complete assess-
ment of the area in question. The second concept states that
• Several tools may be utilized to maximize the
structures within that volume are organized in a constant
utility of volume sonography
relationship to each other.
• MagiCut allows sculpting and refining the
Using VCAD, one can define the spatial relationships of
image
any 2D planes of a particular organ in question, say the fetal
• VCI allows for obtaining thick slices in the A
heart, and then specific software may be utilized to auto-
and C planes
matically generate the specific 2D planes from the acquired
• In general, a VCI thickness of 2 mm is opti-
volume in order to enable full assessment of the area in
mal for the study of the fetal brain (Chaoui
question. This has already been accomplished with the fetal
oral communication 2013)
heart, and the technique is described in a stepwise man-
• It is recommended to utilize VCI on an already
ner in Chapter 11. The same principles can be applied to
acquired volume rather than live, for optimal
any organ, such as the fetal brain or the first-trimester fetus
results (Chaoui oral communication 2013)
(Abu-Rustum et al. 2012). The mid-sagittal volume tech-
• It is possible to color-code the final image
nique for assessment of the first-trimester fetus is described
with respect to a particular application; for
in Chapter 7.
instance whenever TUI is utilized in a vol-
ume, the final image’s color (whenever TUI is
employed) may be set to copper or cool blue,
or any other color (Chaoui oral communica-
Fractional Limb Volume
tion 2013)
• OmniView allows any-direction linear and
Fractional limb volume (FLV) is a novel sonographic tool
curvilinear multislicing within a volume at
based on the principle that fetal weight may be estimated
various thicknesses
from the limb volume (Lee et al. 2004, 2009). By obtain-
• In general, an OmniView line set to a VCI
ing a volume of the fetal thigh or arm, specific software
slice thickness of 20 mm enables optimal
may be employed which allows the sonographer to obtain
evaluation of the fetal spine (Benoit oral com-
several trace-measurements of the limb in question in order
munication 2012)
to calculate the fetal weight. This is described in detail in
• VOCAL enables volume calculation of
Chapter 15.
structures
• SonoAVC facilitates evaluation of multicystic/
fluid-filled structures
Conclusion
• VCAD allows an assessment of the fetal heart
and outflow tracts
Once a volume is acquired, the sonographer may need to
• Fractional limb volume allows fetal weight
apply any combination of several tools to highlight the
estimation from a limb volume
area under evaluation, remove obscuring structures, and
employ modalities to help facilitate volume calculation and
7 Clinical Applicability in the First Trimester
Introduction acquired along the mid-sagittal plane, the same plane utilized
for measuring the nuchal translucency. First-trimester presets
The applicability of volume sonography in the first trimester may be used and the volume may be acquired with an angle
is unique in that a single volume of the entire fetus may be of acquisition of 65 degrees. Subsequent to that, the volume
obtained in one sweep (Michailidis et al. 2002; Fauchon et is standardized in plane A in order to depict the plane of the
al. 2008; Bharudi et al. 2010; Antsaklis et al. 2011; Borrell et abdominal circumference in plane B, from which parallel shift
al. 2011). From the volume it is possible to retrieve planes to is then utilized to navigate cephalad through the volume in
evaluate fetal anatomy and measure the crown–rump length, order to visualize the fetal heart, upper limbs, facial bones,
limb lengths, biparietal diameter, head circumference, and orbits, plane of the biparietal diameter, and the plane of the
abdominal circumference (Abu-Rustum et al. 2012). butterfly, and caudad in order to visualize the fetal kidneys,
cord insertion, bladder, and lower limbs. Table 7.1 covers the
steps of the mid-sagittal volume technique (Figures 7.1–7.14).
Clinical Utility
There are several particular benefits to volume sonography Single-Volume Technique to Evaluate the Fetal Heart
in the first trimester and these are the focus of this chapter.
With the small size of the fetal heart and the proximity of
the 2D anatomical planes – the fetal stomach, four-chamber
view, and three-vessel view – it is possible to examine these
Benefits of Volume Sonography planes, as well as several other transverse cardiac planes,
in the First Trimester from a single volume. Using the first-trimester cardiac pre-
1. Mid-sagittal volume technique for anatomic set, it is possible to acquire a volume of at least 20 degrees at
and biometric assessment the level of the four-chamber view and employ color Doppler
2. Single volume technique for evaluating the or HD-Flow (which may be superior to color Doppler for the
fetal heart smaller vessels in the first trimester). The volume may be dis-
3. Volume NT played using TUI, which enables visualization of the plane of
4. Sonoembryology the abdominal circumference with a visible stomach (estab-
lishing fetal situs), as well as the planes of the four-chamber
view and the three-vessel view in addition to several other
transverse cardiac planes. Standardization of evaluating the
Mid-Sagittal Volume Technique first-trimester heart from a single volume using STIC modal-
ity with color Doppler was first described in 2009 (Turan
The mid-sagittal volume technique was described in 2012 et al.) and enables full cardiac assessment in up to 85% of
(Abu-Rustum et al.) in which a single volume of the fetus is fetuses (Table 7.2; Figures 7.15–7.18).
Table 7.1 Steps for the Application of the Mid-Sagittal Volume Technique
Step 1: The volume is acquired from a sagittal plane with an angle of acquisition of 65 degrees (Figure 7.1)
Step 2: The volume is then standardized in reference plane A via rotation along the X, Y, and Z axes to optimize the depiction of the fetus in the
mid-sagittal plane (Figure 7.2)
Step 3: In reference plane A, the reference dot is then placed on the fetal spine at the level of the diaphragm, automatically generating the axial plane
of the fetal abdominal circumference, with a visible stomach, in plane B (Figure 7.3)
Step 4: Plane B is then selected as the reference plane, and rotation along the Z axis is employed to optimize the location of the spine to 12 o’clock
(Figure 7.4)
Step 5: Parallel shift is then utilized to navigate cephalad within the volume, from reference plane B, to generate six anatomic planes
(Figures 7.5–7.10)
Step 6: Parallel shift is then utilized to navigate caudad within the volume, from reference plane B, to generate four anatomic planes
(Figures 7.11–7.14)
49
50 A Practical Guide to 3D Ultrasound
Stomach
Reference Dot
Upper Limbs
Stomach
Facial Bones
Heart
Orbits
Butterfly
Figure 7.8 Scrolling further cephalad, the fetal orbits and even Figure 7.10 Further cephalad, the plane of the butterfly, formed
the lenses may be seen. by the choroid plexus filling the lateral ventricles, is reached.
Kidneys
Cord Insertion
Bladder
Figure 7.12 Scrolling further caudad, the cord insertion may be Figure 7.13 Scrolling further caudad, the fetal bladder may be
visualized. seen.
Lower Limbs
Figure 7.14 At the level of the bladder and scrolling even fur-
ther caudad, the fetal lower limbs may be seen.
Table 7.2 Steps for the Application of the Single Volume Technique for Evaluating the Fetal Heart
Step 1: The volume is acquired from a transverse plane at the level of the four-chamber view, with HD-Flow, using an angle of acquisition of 55
degrees (Figure 7.15)
Step 2: The volume is then standardized in reference plane A via rotation along the Z axis in order to place the fetal spine at 6 o’clock and the
cardiac apex to the left of the image (Figure 7.16)
Step 3: In reference plane A, the reference dot is then placed at the crux of the heart (Figure 7.17)
Step 4: Plane A is then selected as the reference plane and TUI at an interslice thickness of 1.2 mm and set to 15 slices is used to display the
volume (Figure 7.18)
Step 5: From the displayed volume, the planes of the abdominal circumference with a visible stomach, the four-chamber and three-vessel view
become apparent (Figure 7.18)
54 A Practical Guide to 3D Ultrasound
Fetal Spine
Reference Dot
Ao
3VV
Figure 7.18 The vol- PA
ume is then displayed
using TUI set at 15 slices
1.2 mm apart. Through
this display, it is possible RV
to see the fetal stomach
RA
(S), the left-sided aorta LV
in cross-section (Ao), the LA
four-chamber view with FO
the ventricles and atria
(RV, LV, RA, and LA),
the foramen ovale (FO),
and the three-vessel view
Ao
(3VV) with the aorta
(Ao) and pulmonary S
artery (PA).
56 A Practical Guide to 3D Ultrasound
Volume Nuchal Translucency may be obtained and it can be studied at various gestations,
as has been described by Kim et al. (2008), for the potential
Volume nuchal translucency (NT) is a specific volume-based early recognition and identification of underlying central ner-
software available on select ultrasound machines in which vous system abnormalities.
a volume of the first-trimester fetus is acquired in the mid-
sagittal plane. After acquisition of the volume and using the
applicable presets on the machine, there is automatic gen- Limitations of Volume Sonography in the
eration of an optimized, magnified mid-sagittal image of the Evaluation of the First-Trimester Fetus
fetal head and thorax (Figure 7.19). Subsequently, the opera-
tor places a box over the optimal area for measuring the NT Although volume sonography has great advantages in the
for automatic generation of the fetal NT. first trimester, facilitated by the ability to obtain a single vol-
ume of the entire fetus for later off-line analysis, there remain
several limitations. At this point in gestation the fetus is often
Sonoembryology in a flexed position, with the upper limbs obscuring the face.
In addition, there tends to be significant fetal motion beyond
Another in vivo application for volume sonography in the 13 weeks, resulting in artifact introduction. As a result, the
first trimester is to facilitate the study of the fetal ventricu- optimal time for volume acquisition is after 12 weeks, when
lar system (Figure 7.20). This requires expertise and a clear the fetus is in a near-still sagittal lie. One must also keep in
understanding of fetal embryology. By applying the inversion mind the developmental limitations, such as normal fetal gut
mode, and possibly employing SonoAVC to volumes of the herniation, in order to avoid misdiagnoses which could cause
developing fetal brain, a cast of the fetal ventricular system undue parental anxiety.
Figure 7.20 A transvaginal volume of an 8w4d fetus is acquired and displayed using TUI at an interslice thickness of 0.5 mm and with
VCI at a slice thickness of 1 mm depicting the developing ventricular system.
Figure 7.21 From a single 3D volume of a first-trimester fetus, it is possible to generate all the planes required for an anatomic
and biometric assessment (RK and LK, right and left kidneys; O, orbits).
Practical Pearls
• To maximize the success of retrieving all the • It is possible to automatically generate the plane
respective anatomic and biometric planes out of a for measuring the fetal NT out of an acquired
single volume, start with as true a mid-sagittal lie volume and to utilize specific software to auto-
as possible, optimize the 2D settings, acquire the matically measure the optimal NT using certain
volume with an angle of 65 degrees sonographic machines
• Standardize the volume at the level of the abdomi- • Applying the inversion mode to a volume of the
nal circumference plane and scroll cephalad as first trimester fetal brain allows the generation of
well as caudad for a full assessment of the fetus in a cast of the fetal ventricular system
the first trimester • In the first trimester and with the small size of the
• For evaluating the fetal heart, acquire a 3D vol- fluid-filled structures, it may be easier to utilize
ume starting at the level of the four-chamber view SonoAVC follicle (Benoit oral communication
using HD-Flow with an angle of acquisition of 55 2012) to invert key structures in the brain and
degrees abdomen
• Display the volume using TUI at 12-15 slices 1.2–2 • VCI is most helpful in the analysis of a first tri-
mm apart in order to establish fetal situs by visual- mester volume
izing the plane of the abdominal circumference as
well as the planes of the four-chamber view and
the three-vessel view
8 Clinical Applicability in the Fetal Face
Introduction
Facial Abnormalities Where Volume
Nowhere is the beauty of volume sonography more appar- Sonography is of Added Value
ent than in the evaluation of the fetal face, especially today 1. Facial clefts
with the availability of HDlive (Figure 8.1). The fetal face 2. Facial tumors
is an area where 3D ultrasound has been proven to be of 3. Orbital abnormalities
added clinical value in comparison to 2D sonography. In 4. Nasal abnormalities
1995 Devonald et al. described quasi-3D imaging as com- 5. Maxillary/mandibular abnormalities
plementary to 2D imaging in the evaluation of the fetal face 6. Neck abnormalities
(Devonald et al. 1995), followed by Merz et al.’s report using 7. Other
transabdominal and transvaginal 3D ultrasound to detect or
exclude facial abnormalities in 618 fetuses between 9 and
37 weeks. Merz concluded that 3D ultrasound provided
convincing evidence for its use in the evaluation of normal Facial Clefts
and abnormal fetal anatomy (Merz et al. 1997). However,
imaging of the fetal face has been one of the main rea- While the patient and family members are eager to see the
sons for the improper utilization of volume sonography for fetal face, imaging of this structure by the physician is impor-
“entertainment ultrasound,” and has resulted in abuse by tant to exclude facial abnormalities that at times may be iso-
some sonographers and physicians who have capitalized on lated or may present as part of a syndrome. The area that has
the emotional component of 3D imaging. The purpose of been studied extensively, using 3D ultrasound, is the prenatal
this chapter is to demonstrate the value of 3D ultrasound diagnosis of facial clefting. Although a cleft lip can be easily
beyond just the “pretty face,” where much skill needs to be visualized by surface rendering after artifactual shadowing
acquired and many techniques need to be mastered to use has been excluded from the cord, placenta, limbs, or digits
volume sonography to its fullest potential in evaluating the (Figure 8.2), the hard and soft palate prove to be much more
fetal face. difficult to image.
Clinical Utility
59
60 A Practical Guide to 3D Ultrasound
Figure 8.4 3D
volume of a
20w4d fetus with
multiple anoma-
lies. (A) Volume
is displayed in
the multiplanar
mode using skel-
B
etal mode. The
reverse-face tech-
nique is used to
show bilateral
deep cleft pal-
ates (arrows). (B)
A Volume is dis-
C
played using sur-
face mode, clearly depicting a frontal encephalocele, which mimics an orbital tumor and left exophthalmos. These images helped clarify the
complex anomalies to the family. (C) Postmortem image confirming the findings of a deep right cleft lip and palate, a left cleft lip and palate,
and left exophthalmos. The encephalocele ruptured during delivery (postnatal image courtesy of Adba Frangieh, MD).
Clinical Applicability in the Fetal Face 61
The clinician can use several imaging approaches to iden- shadowing anteriorly from a limb, the cord, or the placenta.
tify the facial structures such as the reverse-face (Figure 8.3 In 2005, Campbell et al. reported on the use of this tech-
and 8.4), flipped-face (Figure 8.5), OmniView (Figure 8.6), nique in eight cases of facial clefting (Campbell et al. 2005)
oblique face, or a modification of all the above. The gold with a high degree of diagnostic accuracy. However, a cleft
standard for the proper technique has yet to be established. in the soft palate was missed in one case.
Additional key points to keep in mind are how to acquire the In 2004, Rotten carried out a systemic analysis of the fetal
image plane for evaluation of the fetal face. Options include face on 10,500 fetuses. Using 2D, a true mid-sagittal plane
the standard mid-sagittal view, the axial or coronal view. was acquired, and subsequently a coronal view, for a thor-
The reverse-face technique was described by Campbell ough evaluation of the fetal face. However, using 3D and 4D
and Lees (2003) (Table 8.1). In this technique, an attempt allowed for an easier, more rapid, and more accurate assess-
is made to acquire a volume commencing from the sagittal ment of the normal fetal face (Rotten and Levaillant 2004a).
plane, display it in the multiplanar mode, and then rotate Rotten then carried out one of the largest case series, on 96
the image in plane A by 180 degrees along the vertical Y fetuses with various facial clefts. This was a retrospective
axis. The render box is subsequently placed in the back-to- review in which it was demonstrated that 3D/4D was superior
front orientation to visualize the palate by scrolling through to non-3D/4D imaging (Rotten and Levaillant 2004b).
the volume. The benefit of this technique is avoiding any
62 A Practical Guide to 3D Ultrasound
In the flipped-face technique described by Platt in 2006 shadowing. As with the reverse-face technique, the ability to
(Table 8.2), a 3D volume is obtained with the fetus in the supine visualize the soft palate is limited (Platt et al. 2006).
position and displayed in the multiplanar mode. Subsequently, Benacerraf et al., in 2006, described a case of Fryn’s
the image in plane A is flipped by 90 degrees so that the fetus syndrome in which the fetus had multiple abnormalities.
is now vertical with the chin up. The render box is then placed Here, 3D and fetal magnetic resonance imaging (MRI) were
over the mandible, the size minimized to enhance resolution, employed. Using the en-face thick-slice (VCI) technique, a
and the volume is scrolled through from the chin to the nose. cleft palate was detected which proved key to the prenatal
The main limitation in this technique is acquisition without diagnosis of Fryn’s syndrome (Benacerraf et al. 2006).
Clinical Applicability in the Fetal Face 63
In 2007 Faure introduced yet another technique, ante- Pilu described a novel technique for the palate: angle of
rior axial 3D view, seen from the underside to visualize insonation with 3D. This technique was used in 15 normal
the secondary palate. The key differentiating factor for this fetuses at 19–28 weeks and one fetus with a cleft at 33
technique is that the volume is acquired from the axial and weeks (Pilu and Segata 2007). The main goal of this tech-
not the mid-sagittal plane, as in the previously described nique was to insonate at a 45-degree angle to avoid shad-
reversed- or flipped-face techniques. In the prospective study, owing from the alveolar ridge. The modes used were the
Faure assessed 100 fetuses at 17, 22, 27, and 32 weeks. With multiplanar, surface display (maximum mode) in addition
the transducer just in front of the alveolar ridge, all aspects to TUI and VCI. The authors concluded that in normal
of the posterior palate were studied by visualizing seven fetuses, the axial and coronal acquisitions were as helpful,
defined anatomic landmarks. Sonographic findings were sub- but in the abnormal cases, the coronal acquisition proved
sequently compared to surgical fetopathological specimens. to be more helpful. However, the authors remained uncer-
The ideal time for utilizing this technique was determined to tain as to this technique’s utility in isolated clefts of the
be at 20–24 weeks (Faure et al. 2007). soft palate.
64 A Practical Guide to 3D Ultrasound
McGahan et al. in 2008 used the 3D multislice display In 2008 Zoppi et al. reported on an isolated case of a cleft
(TUI) to help identify facial clefts. The technique was stan- palate in a high-risk patient who had been missed on routine
dardized in both the axial and sagittal planes. This enabled sonographic evaluation. However, re-evaluation of the stored
full visualization of the fetal face from the palate to the orbits volume, using an axial 3D reconstruction, enabled visualiza-
in nine slices, where the interslice thickness was set at 3.7 tion of the cleft (Zoppi et al. 2008). From this report, one can
mm (McGahan et al. 2008). infer that even if an isolated cleft palate is missed on rou-
tine evaluation, if there is a suspicion of a cleft palate, the
Clinical Applicability in the Fetal Face 65
examiner could carry an off-line re-examination of the vol- As a result of the availability of so many different tech-
ume, utilizing all the available techniques, to further deter- niques with which to evaluate the face, a study was carried out
mine the presence or absence of a cleft palate. If that were to by Martínez Ten in 2009 to compare the various techniques
be confirmed, the parents would be re-contacted to make the for visualization of the soft palate (Martínez Ten et al. 2009).
necessary arrangements for follow-up and further care and Ten fetuses with clefts and 50 normal fetuses, at 20–33 weeks
management. of gestation, were evaluated. The authors concluded that in
Faure et al. in 2008 noted that the arching of the soft pal- order to visualize the soft palate, a near-perfect volume must
ate puts it in a different plane than the hard palate, which be obtained with a good fluid interphase between the fetal
contributes to the inadequacy of its visualization. They sug- tongue and palate. The oblique and flipped-face techniques
gested that this can be avoided by employing the 30 degree, proved to be the superior techniques.
3D-inclined axial view. This was evaluated on 87 low-risk In 2009 Wong et al. re-examined the fetal palate from
fetuses at 21–25 weeks, in which a volume was obtained stored volumes of 31 normal fetuses at 15–35 weeks. It was
for examination of the soft palate. The images were subse- determined that visualizing the uvula, which corresponds to
quently compared to pathological specimens. Although this the soft palate, is most difficult at less than 19 weeks and
technique’s reproducibility was not evaluated, it was found to beyond 35 weeks, when the angulation of the arch is even
be of utility in assessing intactness of the soft palate (Faure greater, putting it in a more difficult plane to access in com-
et al. 2008). parison to the plane of the hard palate (Wong et al. 2009).
66 A Practical Guide to 3D Ultrasound
Most recently, in 2012 Tonni et al. reported on the In 2005 Paladini et al. used volume sonography on a cav-
“OmniView Algorithm” as a new 3D technique for the ernous hemangioma of the face and neck. This was of utmost
study of the fetal hard and soft palates, in which it is pos- utility in counseling the family, and in consultation with the
sible to simultaneously display three nonorthogonal planes surgeons to plan care for this fetus (Paladini et al. 2005).
commencing from a fetus in a mildly flexed position (Tonni Another report on a palatal teratoma by Merhi et al. in
et al. 2012). Ideally, there needs to be fluid in the orophar- 2005 concluded that 3D and color Doppler helped clarify the
ynx and the absence of the cord or limbs from in front of extent of the teratoma, which may have been missed by 2D,
the face. Here, skeleton mode is used to acquire the vol- and determined that there was no need for an EXIT proce-
ume from the top of the head to the chin, using an angle dure. This facilitated planning of intrapartum/postpartum
of roughly 65 degrees. The OmniView algorithm is then care (Merhi et al. 2005). In contrast, Shih et al. reported on
employed utilizing three polylines. The first line is drawn the use of 3D and MRI in the case of an oral tumor, an epig-
from the posterior aspect of the palate down to the chin, nathus, and in this case it helped prepare for an EXIT proce-
generating an image of the labia, alveolar ridge, and the dure by clarifying the extent of the tumor and the obstruction
uvula (indicating an intact palate). The second line is drawn to the airway (Shih et al. 2005). Sherer et al. reported a simi-
from the anterior and posterior nasal spines to the tip of lar case in 2006 where, again, 3D of a massive fetal epigna-
the uvula. This generates an image that shows the labia and thus helped in the decision regarding an EXIT procedure by
alveolar ridge. The third is a vertical line extending behind delineating the extent of the tumor (Sherer et al. 2006).
the frontal bone down to the chin, the equivalent of the
reverse mode. This generates an image of the hard palate
and tongue (Figure 8.6). Orbital Abnormalities
In summary, the ideal technique for the evaluation of
the fetal face for the various types of clefts has yet to be Although orbital abnormalities (Figure 8.4) are not that
ascertained. For this reason, it is important to be aware of common, they do carry serious implications. In 2000,
all the available techniques and when indicated, whether Blaas et al. reported on a nine-week fetus with holopros-
because of history, current suspicion, or the mere pres- encephaly, cyclopia, and a proboscis (Figure 8.15) using
ence of a cleft lip, to employ these various modalities in an transvaginal scan “any plane” 3D slicing technique. This
attempt to ascertain intactness or involvement of the hard enabled reconstruction of facial planes otherwise unavail-
and soft palates. able through 2D and provided valuable additional informa-
tion (Blaas et al. 2000b).
Facial Tumors
Clinical Utility of Volume
There is a multitude of facial tumors where volume sonog- Sonography in Orbital Abnormalities
raphy has been utilized to further characterize the mass in 1. Ascertaining the presence of cyclopia,
question, and to aid in planning the intrapartum and postpar- anophthalmia
tum care of these babies. One of the earliest reports was by 2. Ascertaining the presence and extent of
Shaw et al. in 2004 in a case of congenital epulis, a gingival dacrocystoceles
granular cell tumor. In this case, 3D aided in the visualiza-
tion of the mass; however, it was misleading in giving the
impression that an EXIT procedure was needed, where in Sepulveda et al. reported on 10 cases of congenital dac-
reality it was not (Shaw et al. 2004). An EXIT procedure rocystocele. In 3/10 cases, volume sonography was used
(ex utero intrapartum treatment) is performed at the time and helped clarify the abnormality. This was in terms of the
of cesarean delivery whenever fetal airway obstruction is extent of the dacrocystocele’s extension into the nasal cavity
suspected. Using EXIT, the fetal airway is secured prior to as well as any connection between the nasal cavity and the
clamping the umbilical cord. orbits. The results were comparable to MRI and deemed wor-
thy of considering 3D as the standard for scanning in these
cases (Sepulveda et al. 2005).
Clinical Utility of Volume Johnson et al. used 3D in a case of oculoauricularfrontonasal
Sonography in Facial Tumors syndrome. In this case, 3D provided invaluable information to
1. Sizing of the tumor the couple in appreciating the abnormality (Johnson et al. 2005).
2. Assessing extent of airway involvement and Most recently, Wong et al. used the reverse-face view to
determining the need for an EXIT procedure visualize a case of anophthalmia. The benefit of this tech-
nique was in eliminating the shadows and clarifying the
abnormality (Wong et al. 2008).
Clinical Applicability in the Fetal Face 67
NB
A B
Figure 8.16 3D volume of a 22w6d fetus. (A) Volume displayed using surface rendering. (B) Subsequently, the volume is displayed in
the maximum mode, clearly depicting both nasal bones (NB).
68 A Practical Guide to 3D Ultrasound
A B
Figure 8.17 3D volume of a 22w0d fetus with microretrognathia is obtained. (A) Volume is displayed in the three orthogonal planes.
Note the reference dot localizing the nasal bone in all three planes. Note the mandible (*) in plane A. (B) Volume is rendered using the
surface mode, clearly depicting the microretrognathia.
Clinical Applicability in the Fetal Face 69
Neck Abnormalities
Clinical Utility of Volume
One of the earliest reports on the use of volume sonogra- Sonography in Evaluating
phy was describing facial tumors and differentiating a cystic the Fetal Neck
hygroma from a thickened nuchal translucency (Figure 8.18 1. Characterizing neck tumors and differenti-
and 8.19). Bonilla-Musoles et al. rescanned 25 fetuses and ating a cystic hygroma from a thick nuchal
used volume sonography to characterize their neck masses. translucency
Characteristics used were bullae as well as the extent, ampli- 2. Proper sizing of fetal goiter and determining
tude, and the lack of membrane regularity, to further define the extent of response to therapy
the malformation as a cystic hygroma or a nuchal translu-
cency. It was concluded that 3D was helpful in 70% of the
cases (Bonilla-Musoles et al. 1998).
A B
Figure 8.18 3D volume of a 16w5d fetus with a septated cystic hygroma. (A) Volume is displayed in the multiplanar mode. (B) Volume
is displayed using TUI at an interslice thickness of 2 mm and VCI at a slice thickness of 2 mm, and using sepia as the color. The reference
dot is placed in the largest cyst, localizing it in all eight panes.
A B C
Figure 8.19 A transvaginally acquired volume of 9w3d fetus with a visible nuchal translucency. (A) Fetus in 2D showing the NT. (B) NT
as seen utilizing surface rendering. (C) NT as seen using HDlive render mode.
70 A Practical Guide to 3D Ultrasound
A fetal goiter was examined by 3D and power Doppler In addition, and due to the complexity of the evaluation of
angiography by Nath et al. The true benefit was in following the fetal face, Roelfsema et al. have developed a comprehensive
its volume and response to therapy, but most importantly, in detailed sonographic technique for establishing fetal craniofa-
aiding the parents to appreciate the goiter, and this proved to cial biometry. This craniofacial variability index (CVI) con-
be the major incentive for their compliance (Nath et al. 2005). sists of 16 different measurements of the fetal face. For their
evaluation, 136 normal fetuses and six abnormal fetuses were
evaluated by volume sonography at 18–34 weeks of gestation.
Other Uses of Volume Sonography Anthropometry and cephalometry were utilized in establish-
in Evaluation of the Fetal Face ing Z scores. The study concluded that when, in the absence
of intrauterine growth retardation, two or more abnormal Z
Several other areas in the fetal face have been evaluated by scores are present, this may be indicative of dysmorphology
volume sonography, as listed below. (Roelfsema et al. 2007a). In a subsequent study by the same
group on seven syndromic fetuses and seven with isolated
facial clefts, a higher CVI was found in the more severe bilat-
eral clefts. In addition, CVI was higher and there were more
abnormal Z scores in the syndromic fetuses versus those with
isolated clefts. The conclusion was that this could be a differ-
Other Uses for Volume Sonography entiating method between syndromic fetuses and those with
in the Evaluation of the Fetal Face isolated facial clefts (Roelfsema et al. 2007b).
1. Ectodermal dysplasia In summary, the fetal face, a most elusive, complex area
2. Congenital ichthyosis “Harlequin” fetus of the fetus, can undergo extensive evaluation with the use
3. Determining the in-utero craniofacial vari- of volume sonography. The key is to look beyond the “pretty
ability index (CVI) face,” become familiar with the complex techniques, and
4. Dysmorphologies: cebocephaly, trisomies, oto- know when to employ them in order to differentiate syn-
cephaly, Treacher Collins, cat-eye syndrome dromic cases from those with isolated abnormalities.
Several case reports have concluded that 3D is helpful in visu- Though volume sonography certainly helps clarify several
alizing the details of the face, ears, and lips in confirming complicated facial abnormalities and may help provide more
ectodermal dysplasia, trisomy 18, frontonasal malformations, evidence to a potential underlying chromosomal aberration
cat-eye syndrome, cebocephaly, otocephaly, cases of unusual (Figure 8.20), it nonetheless may provide false reassurance.
facial clefting, and Treacher Collins syndrome. The greatest Caution must be exercised in cases of trisomies where a 3D-
benefit was in helping the parents appreciate the abnormality rendered image may be highly suggestive of a normal fetus
(Lin et al. 1998; Hsu et al. 2002; Shipp et al. 2002; Tanaka et with no discernable facial features to suggest a fetus affected
al. 2002; Sepulveda et al. 2003; Volpe et al. 2004; Pilu et al. by trisomy 21. This is precisely why the suspicion should
2005; Allen and Maestri 2008; Allen et al. 2008; Zheng et al. rely on the well-established basic 2D sonographic markers.
2008). In addition, although volume sonography has been shown to
Another utility for volume sonography has been demon- be of value in certain cases of skin abnormalities such as in
strated by Benoit (1999), Bongain et al. (2002), and Vohra et the “Harlequin” fetus (Bongain et al. 2002), it has not been
al. (2003): the prenatal diagnosis of congenital ichthyosis, the shown to be of diagnostic value in cases of skin denudation
“Harlequin” fetus. This is a rare congenital abnormality that syndromes (Abu-Rustum et al. 2013) (Figure 8.21).
cannot be diagnosed by 2D alone. Utilizing volume sonog-
raphy enables confirmation of the typical “fish mouth” and
fixed upper extremities.
Clinical Applicability in the Fetal Face 71
A B
Figure 8.20 3D volume of a 21w2d fetus with suspected trisomy 21. (A) 2D image of the fetal profile with an abnormally close man-
dibular-maxillary line (dotted line) and prenasal thickness (*). (B) Volume displayed using HDlive depicting the up-slanting palpebral
fissures and small nose. This fetus was confirmed to have Down syndrome.
Conclusion in mind the various artifacts that may be introduced and that
might ultimately lead to false diagnoses or reassurances.
Volume sonography has an important role in the clarification Therefore the user must be familiar with the available tech-
of abnormalities involving the fetal face. It also has a great niques and should gain expertise in utilizing them in normal
role in early reassurance, which may be possible from the fetuses in order to be able to properly utilize them in cases of
first trimester, to ease the anxiety of families having prior a suspected abnormality. The gold standard remains a good
affected offspring (Figure 8.22). The greatest benefit is in the 2D image. Any suspicion of a facial abnormality may be clar-
extensive evaluation of facial clefts. Nonetheless, the tech- ified further with the proper utilization of 3D sonography.
niques are complicated, require expertise, and one must keep
Practical Pearls
Introduction
Utility of Volume Sonography
The brain is one of the most challenging areas to image in the in CNS Evaluation
fetus. This is due to the fact that for a full evaluation, several 1. Sonoembryology
planes are required, and those planes are not parallel to each 2. Skull
other. Some of these planes are oblique, making the evalu- 3. Cranial sutures
ation difficult. In addition, there is the challenge of obtain- 4. Corpus callosum
ing the mid-coronal plane, and this further limits a complete 5. Vascular malformations
assessment. With the advent of volume sonography, visual- 6. Other areas
izing all these planes can be facilitated if one were to obtain
a 3D volume of the brain and then properly navigate through
it, utilizing the various available tools and techniques.
Sonoembryology
Clinical Utility Several authors have looked at the role of volume sonography
in fetal development. One of the earliest studies was by Blaas
Although a good 2D image remains the mainstay and the et al. (1995) in which they were able to visualize structures of a
basis for a good 3D image, numerous studies have addressed few mm using 3D sonography. Viñals et al. used volume- con-
the utility and advantages of volume sonography for the fetal trast imaging (VCI) on 203 fetuses to establish normograms for
central nervous system (CNS). The primary areas of inter- the developing cerebellar vermis at 18–23 (Viñals et al. 2005).
est that have demonstrated added benefit are those involv- In 2007, Mittal et al. used volume sonography to look at the
ing sonoembryology and characterizing normal development development of the sylvian fissure starting at 12 weeks. They
(discussed in Chapter 7), evaluating the cranial sutures were able to identify 99% of sylvian fissures from 12 weeks on
(Figure 9.1), the corpus callosum (Figure 9.2), angiography (Mittal et al. 2007). Sepulveda et al. used 3D sonography to
of vascular malformations, as well as clarifying subtle differ- ascertain holoprosencephaly at 9w6d (Sepulveda et al. 2007)
ences, leading to more accurate diagnoses in CNS anomalies. (Figure 9.3). Roelfsema et al. reported on the use of 3D for
73
74 A Practical Guide to 3D Ultrasound
Cavum Septi
Pellucidi
Corpus Callosum
A B
Figure 9.3 TUI of a normal and an abnormal brain. (A) TUI of a 12w5d normal fetal brain at an interslice thickness of 0.6 mm and a
VCI thickness of 2 mm, depicting the “butterfly” formed by the choroid plexus filling the lateral ventricles. (B) TUI of a 12w6d abnormal
fetal brain with holoprosencephaly at an interslice thickness of 0.6 mm and a VCI thickness of 2 mm. Note the absence of the butterfly, and
the single ventricle (*).
Clinical Applicability in the Fetal Central Nervous System 75
The Skull
Clinical Utility of Volume
3D ultrasound helps clarify various anomalies of the bony Sonography in Evaluating the Skull
skull, namely in cases of acrania and encephaloceles. Various 1. Ascertains the intactness of the skull
modalities may be used, with the maximum mode being the 2. Helps determine the extent of involvement of
most applicable, in order to show the bony defect. It is also the brain and spine in case of a malformation
possible to combine TUI with VCI in addition to surface ren- 3. Clarifies the anomaly to the family
dering. Care must be taken in these cases, as the images gener-
ated may sometimes be quite unsettling for the family, and it is
advisable to check with the family whether they prefer not to
see any “colored” images. In such cases, off-line analysis may
be carried out on stored volume data sets (Figures 9.4–9.6).
*
A B
Figure 9.6 3D volume of a
15w3d fetus with a cystic structure
posterior to the head. (A) Volume *
displayed in the multiplanar mode
with surface rendering using *
HDlive, confirming the presence
of a posterior encephalocele. (B)
Close up of the defect (*). A B
76 A Practical Guide to 3D Ultrasound
Clinical Utility of
Volume Sonography in
Figure 9.11 The
Evaluating the Sutures
single-pane view is
1. Differentiating molding from craniosynostosis selected to visualize
2. Visualizing the entire length of the suture line the metopic suture
3. Measuring the size of the anterior fontanelle (*) of the 21w2d
fetus.
78 A Practical Guide to 3D Ultrasound
CSP CC
CSP CC
A B
Figure 9.12 3D volume of a 27w1d fetus. (A) Volume acquired from the axial plane, plane A, and displayed in the multiplanar mode,
automatically generating the sagittal plane in plane C. Plane C shows the corpus callosum (CC) and the cavum septi pellucidi (CSP). (B)
Single-pane view is now selected, with a clearly visualized corpus callosum and cavum septi pellucidi. This is a difficult plane to obtain
during routine scanning, and navigation through a properly acquired 3D volume facilitates ascertaining the presence of the corpus callosum.
Clinical Applicability in the Fetal Central Nervous System 79
CB
CC
Th
CSP
Falx
CSP
A Vp C
CSP
CB
CC
D
V
B
Figure 9.13 Accessing difficult planes in a 22w0d fetus. (A) Volume displayed in TUI at an interslice thickness of 2 mm and VCI with
a slice thickness of 2 mm, showing the axial structures. (B) The same volume is now displayed using the multiplanar mode, automatically
showing the challenging sagittal plane in plane C. (C) Using OmniView, the corpus callosum is seen. (D) Centering the render box over
the midline generates a view of the corpus callosum using HDlive. CB, cerebellum; Th, thalami; F, falx; CSP, cavum septi pellucidi; Vp,
posterior horn of the lateral ventricle; V, vermis; CC, corpus callosum.
Figure 9.14 3D volume of a 19w4d fetus with hydranencephaly displayed using TUI at an interslice thick-
ness of 3.1 mm and VCI at a slice thickness of 2 mm. Note the loss of normal architecture and the extent of
involvement.
80 A Practical Guide to 3D Ultrasound
Other Uses of Volume Sonography in the Fetal CNS superior to 2D for visualizing the transcerebellar axial plane
in 202 fetuses at 16–24 weeks (Correa et al. 2006; Varvarigos
Several other areas involving the role of volume sonography in et al. 2002).
the fetal CNS have been studied. Those have involved midline Pilu et al. found that although 2D had better quality in
structures, characterizing choroid plexus cysts (Figure 9.22) midline anomalies, 3D was easier and as effective for rapid
and the posterior fossa (Volpe et al. 2012) (Figure 9.23) as assessment of the median plane of the head, and most use-
well as further assessing the presence of specific craniofacial ful when 2D proved to be difficult. The main downfall was
abnormalities in particular syndromes. Timor-Tritsch et al. evaluating the brainstem in this study (Pilu et al. 2006). Soto
in 2000 used the transfontanelle 3D view and showed that et al. used 3D as an adjunct to 2D to look at the skull mineral-
it proved to be of great utility for review, consultation, and ization in the absence of the occiput (Soto et al. 2006). Bault
teaching (Timor-Tritsch et al. 2000). Paladini and Volpe used used 3D sonography to examine the optic chiasm (Bault
3D to evaluate the posterior fossa and vermian morphom- 2006). Sepulveda used 3D reconstruction of the fetal skull
etry in order to characterize vermian abnormalities (Paladini and face to characterize the “helmet sign” of the forehead of
and Volpe 2006). Correa et al. found 3D neurosonography a fetus with Wolf-Hirschhorn syndrome (Sepulveda 2007).
82 A Practical Guide to 3D Ultrasound
Figure 9.20 The size of the render box is now adjusted and
enlarged to encompass the entire Circle of Willis. Minimum mode
is selected which removes all gray-scale structures completely and
clearly depicts the vasculature.
Clinical Applicability in the Fetal Central Nervous System 83
Figure 9.22 3D volume of a 21w0d fetus with brachycephaly and bilateral choroid plexus cysts displayed using TUI at an interslice
distance of 1.8 mm and a VCI slice thickness of 1 mm.
84 A Practical Guide to 3D Ultrasound
T
BS BS
Vermis
Vermis
A B
Figure 9.23 3D volume of the brain of a 22w6d fetus. (A) Navigating through the volume it is possible to
generate the plane in which the brainstem–tentorium angle is measured. (B) Navigating through the volume, it
is possible to generate the plane in which the brainstem–vermis angle is measured. This enables assessment of
the posterior fossa for any abnormalities. BS: brain stem; T: tentorium.
Practical Pearls
• Whenever a skull defect is suspected, the maximum • For the evaluation of the posterior fossa and brain-
mode aids in ascertaining the presence of acrania stem, it is helpful to acquire a volume starting with
• A good acquisition of the fetal brain may be obtained an axial plane in which both the cerebellum and
through the transfontanelle window cavum septi pellucidi are seen (Chaoui oral commu-
• Starting with an axial plane, the multiplanar mode nication 2013)
will automatically show the corpus callosum in • Utilizing VCI and TUI is instrumental to high-
plane C quality sectional analysis of the brain along any of
• To avoid bone shadowing when acquiring a volume the 3 axes
of the fetal brain, apply gentle pressure with a steady • Using VCI at a thickness of 2 mm together with the
hand (Paladini oral communication 2013) transparent mode allows optimal visualization of the
• An angle of 35-40 degrees is suitable for acquiring a cerebellum (Chaoui oral communication 2013)
volume of a second-trimester fetal brain • Properly utilizing 3D ultrasound in the evaluation of
• A great advantage to displaying a volume of the fetal the fetal brain provides access to challenging struc-
brain in the multiplanar mode is the ability to study tures and planes, is a great teaching tool and enables
the axial and sagittal planes simultaneously (Pilu off-line consultation
oral communication 2013)
10 Clinical Applicability in the Fetal Skeleton
Introduction
Clinical Utility
1
Rib Cage
2
3
Although it is not routine practice to count the fetal ribs, this
may be of use in certain syndromes. This task is almost impos- 4
sible by 2D ultrasound but has been made possible with the 5
availability of volume sonography. Assessing the number and 6
presence of hemi vertebrae (Figure 10.1) as well as abnormal 7
spacing between the ribs may be of diagnostic value. In 2002 8
Viora et al. reported that 3D sonography helped narrow the Figure 10.2 A 9
differential diagnosis in a fetus with short rib polydactyly 3D volume of
10
(Viora et al. 2002). Sallout et al. reported that 3D sonography the rib cage of a
was complementary to 2D scanning once post-processing was 24w4d fetus ren-
11
utilized to enhance the image (Sallout et al. 2006). Gindes et dered using the
al. reported on the utility of 3D ultrasound in counting the ribs maximum mode
of 75 fetuses and hinted at the possible association between and showing 11
an abnormal number of ribs (Figure 10.2) and childhood ribs.
85
86 A Practical Guide to 3D Ultrasound
The value of volume sonography in studying the fetal spine has as with the rib cage, utilizes the reference dot for navigation
been primarily evaluated with respect to development of the within a volume, and images rendered in maximum mode.
spine and localization of neural tube defects. There have been Table 10.2 describes a traditional multiplanar method for view-
many methods utilized to display the fetal spine. OmniView, ing the spine. Proper localization of the level of the defect in
Clinical Applicability in the Fetal Skeleton 87
A B C
Figure 10.12 Volume of the hand and digits of a 27w0d fetus displayed using three modalities: (A) surface rendering, (B) dynamic
rendering, and (C) HDlive.
Figure 10.16 A
3D volume of a
27w4d fetus with
bilateral club feet
displayed using (A)
Surface rendering
A B
and (B) HDlive.
92 A Practical Guide to 3D Ultrasound
A B
Figure 10.17 A 12w6d fetus with multiple anomalies. (A) 3D volume using surface rendering depicting rhizomelia with proximal short-
ening of the humerus and femur. (B) Postnatal image confirming the findings (postnatal image courtesy of Adba Frangieh, MD).
*
* *
A B C
Practical Pearls
95
96 A Practical Guide to 3D Ultrasound
RA
SVC
A
o
IVC A
DAo
H&N
L
AoA V
O
T
PA
D
A
o
RV
LV
Figure 11.3 A 3D volume of the aortic arch Figure 11.5 A STIC volume of the fetal heart
and descending aorta of a 23w1d fetus. The volume and aortic arch at 23w0d rendered using the
was acquired using power Doppler in the minimum inversion mode and HDlive, depicting the right
mode, hence creating a vascular cast. The aortic and left ventricles (RV, LV) and outflow tracts. PA,
arch, head and neck vessels, and descending aorta pulmonary artery; LVOT, aorta.
are clearly depicted. The final rendered image is
reassuring against the presence of an aortic coarc-
tation. AoA, aortic arch; DAo, descending aorta;
H&N, head and neck vessels.
Clinical Applicability in the Fetal Cardiovascular System 97
AoA
D
A
o
S
N
TV
RV
RA
LV
LA
MV
Figure 11.8 A 3D volume of the heart of a 29w3d fetus is
acquired at the level of the four-chamber view with an angle of
Ao
acquisition of 53 degrees. The volume is subsequently rendered
using surface rendering. Note how clearly the four chambers are
seen (RV, right ventricle; LV, left ventricle; RA, right atrium; LA,
left atrium), the clear off-setting between the tricuspid (TV) and
mitral (MV) valves, and note the left-sided aorta in cross-section
(Ao).
A key point for the evaluation of the fetal heart is obtain- in order to enhance retrieval of the respective anatomic planes
ing the volume with as few extraneous movement artifacts out of a stored volume dataset. This was first described by
as possible (Table 11.1). Optimizing acquisition, minimizing Abuhamad (2004) and is a prerequisite for automation using
shadowing from fetal limbs, and standardizing the display VCAD (Table 11.2).
are key factors in facilitating navigation through the volume
Table 11.2 Steps to Utilizing VCAD for the Evaluation of the Fetal Heart
Step 1: Follow steps 1 through 5 to acquire a standardized volume of the fetal heart as described in Table 11.1
Step 2: Display the volume in the multiplanar mode (Figure 11.10)
Step 3: Select VCAD as a preset which automatically displays the volume in TUI (Figure 11.11)
Step 4: Align the four-chamber view with the schematic representation by magnifying the image and rotating it along the Z axis (Figure 11.12)
Step 5: Align the fetus in plane B with the schematic by rotation along the Z axis (Figure 11.13); this becomes the starting plane (Figure 11.14)
Step 6: Navigate through the volume, utilizing the predefined cardiac planes 1 through 6 for automatic retrieval of the respective cardiac planes
(Figures 11.15–11.20)
Clinical Applicability in the Fetal Cardiovascular System 99
Figure 11.9 A STIC volume of the fetal heart at 22w6d is acquired at the level of the four-chamber view
with color Doppler. The volume is rendered using minimum mode. The ventricles are clearly depicted.
Figure 11.10 Figures 11.10–11.20 exemplify the step-by-step approach to utilizing VCAD to generate
six cardiac planes out of a 3D stored volume data set of the fetal heart using 4D View software. The first
step is to acquire a 3D volume of the fetal heart at the level of the four-chamber view and display it in the
three orthogonal planes with the fetal spine at 6 o’clock and the reference dot (O) placed at the crux of the
heart as shown in plane A.
100 A Practical Guide to 3D Ultrasound
Figure 11.11 Subsequently, TUI is selected with seven images at an interslice distance of 2 mm. The reference
dot (o) is placed at the crux of the heart.
Figure 11.12 VCAD is then activated and the diagrams with which to align the images in planes A and B appear.
Note the malalignment between the schematic and the sonographic images.
Clinical Applicability in the Fetal Cardiovascular System 101
Figure 11.13 The image in plane A is then magnified and rotated along the Z axis in order to align it with the
schematic, and the image in plane B is rotated in order to align the fetal spine with the dotted schematic line.
Figure 11.14 Once the image has been displayed in the optimal standardized format and aligned with the
schematic, the “start plane” button (*) is selected, and now the central image of the four-chamber view becomes the
reference plane for navigating within this volume.
102 A Practical Guide to 3D Ultrasound
LVOT
Figure 11.15 From the standardized reference plane, the cardiac 1 preset is selected which generates the left
ventricular outflow tract (LVOT) in seven planes that are 0.6 mm apart. Utilizing TUI helps correct for the minor
variations between fetuses across gestational ages.
RVOT
Figure 11.16 The cardiac 2 preset is now selected which generates the right ventricular outflow tract (RVOT) in
seven planes that are 1 mm apart.
Clinical Applicability in the Fetal Cardiovascular System 103
Stomach
Figure 11.17 The cardiac 3 preset is now selected which generates the abdominal circumference plane with a
visible fetal stomach. This also helps ascertain fetal situs.
RA
IVC SVC
Figure 11.18 The cardiac 4 preset is then selected which generates the sagittal views of the right atrial inflow
(bicaval view) with the superior and inferior venae cavae (SVC, IVC) inserting into the right atrium (RA).
104 A Practical Guide to 3D Ultrasound
DA
DAo
Figure 11.19 The cardiac 5 preset is then selected which generates the sagittal views of the ductal arch (DA) and
descending aorta (DAo).
AoA
DAo
Figure 11.20 The cardiac 6 preset is then selected which generates the sagittal views of the aortic arch (AoA)
and descending aorta (DAo).
Clinical Applicability in the Fetal Cardiovascular System 105
Perhaps the greatest utility for volume sonography in heart throughout a full cardiac cycle, and combining STIC
the evaluation of the fetal heart is learning the proper fetal with TUI, VCI, inversion mode, or any of the Doppler
cardiac anatomy and how to generate the necessary cardiac modalities enhances the evaluation (Figure 11.23 and 11.24)
planes out of a standardized volume, to facilitate the evalu- and helps reaffirm the location of a ventricular septal defect
ation of the fetal heart using 2D ultrasound. It is possible to (Figure 11.25), ventricular (Figure 11.26), and outflow tract
carry out a near-complete evaluation of the fetal heart from abnormalities (Figure 11.27). In addition, STIC has been
two properly acquired STIC volumes, obtained from an found to be of value in the off-line analysis of first-trimes-
axial and a sagittal sweep, and viewed in cineloop through- ter normal and abnormal fetal hearts (Chapter 7, Table 7.2,
out a full cardiac cycle (Figure 11.21 and 11.22). Numerous Figures 7.15–7.18) in order to generate the basic views and
techniques have been described for studying the fetal heart, characterize any underlying pathology. However, as always
including DeVore’s spin technique, discussed in Chapter 3 with volume sonography, the greatest limitation is the qual-
(Table 3.1, Figures 3.17–3.22), study of the fetal valves in ity of the acquired volume and the route of volume acquisi-
Chapter 4 (Table 4.1, Figure 4.3 and 4.4), and Abuhamad’s tions, whether vaginal or abdominal (Votino et al. 2013). In
VCAD (Table 11.2, Figures 11.11–11.20), among many oth- addition, it is possible to obtain striking surface-rendered
ers. STIC allows the study of a volume of the beating fetal images of the fetal heart (Table 11.3).
3VV
PA
Figure 11.21 A STIC
volume of a 26w6d heart SVC
acquired from the axial
plane and displayed using
TUI with an interslice
LVOT
distance of 1.5 mm. It is
possible to see the four-
chamber view (4CV), the
left ventricular outflow
tract (LVOT), pulmonary 4CV
artery (PA), three-vessel
view (3VV), and superior
vena cava (SVC).
106 A Practical Guide to 3D Ultrasound
IVC
RA AoA
SVC
DAo
Figure 11.22 A sagittally acquired STIC volume of the fetus in Figure 11.21 displayed using TUI with
an interslice distance of 0.5 mm. The aortic arch (AoA), descending aorta (DAo), right atrium (RA), and
superior and inferior venae cavae (SVC and IVC) can be seen.
A B
Figure 11.23 A 3D volume of a 21w2d fetus with an atrioventricular (AV) septal defect. (A) The volume is displayed using TUI at an
interslice thickness of 2 mm and VCI with a slice thickness of 2 mm. The loss of the normal off-set of the AV valves is seen as well as the
atrial (ASD) and ventricular (VSD) components of the defect. (B) The volume is rendered using HDlive, clearly depicting the defect.
Clinical Applicability in the Fetal Cardiovascular System 107
CAT
Left Right
HRV
S
A B
Figure 11.24 A STIC volume of a 22w5d fetus with an atrioventricular (AV) septal defect, a hypoplastic right ven-
tricle (HRV), and a common arterial trunk (CAT). (A) The volume is displayed using TUI at an interslice thickness of 2
mm and VCI with a slice thickness of 2 mm. Normal fetal situs is ascertained by visualizing the fetal stomach (S). The
loss of the normal off-set of the AV valves is seen as well as the ventricular and atrial components of the defect. (B) The
volume is rendered using surface rendering clearly depicting the defect.
VSD
VSD VSD
A
VSD
B C D
Figure 11.25 A series of 2D and 3D images of a second-trimester fetus with an isolated mid-muscular ventricular
septal defect (VSD). (A) A 2D image of the four-chamber view depicting the VSD. (B, C) The location of the VSD is
ascertained using color Doppler. (D) A 3D volume of the fetal heart is now rendered using the inversion mode, clearly
demonstrating the VSD.
Figure 11.27 A 3D
AV
sagittal volume of the
aortic arch and descend-
ing aorta of a 34w0d
fetus with ventricular
FO disproportion. The vol-
AV
ume is rendered using
the inversion mode with
HDlive. This was a case
Figure 11.26 A 3D volume of a 15w3d of coarctation of the aorta
fetus with a univentricular heart rendered further clarified utilizing
using the inversion mode during diastole. Note the inversion mode. Note
the flow across both atrioventricular valves the location of the luminal
(AV) as well as across the foramen ovale (FO). narrowing (*).
108 A Practical Guide to 3D Ultrasound
Figure 11.28 A 3D volume of the fetal heart at the level of the four-chamber view
obtained using the cardiac preset, and displayed in the multiplanar mode.
Figure 11.29 The volume is rendered using surface rendering with a direction of back-to-
front selected in plane B for viewing the region of interest.
Clinical Applicability in the Fetal Cardiovascular System 109
Figure 11.30 The size of the render box is adjusted in order to optimize the final rendered
image of the four-chamber view.
MB
TV
MV
Ao
Figure 11.31 The single-pane display is selected and the Figure 11.32 HDlive surface rendering is then selected,
threshold and mix are adjusted in order to optimize the final with which the final rendered image is displayed. Note the left-
rendered image. sided aorta in cross-section (Ao), the normal off-setting of the
atrioventricular valves (MV, mitral valve; TV, tricuspid valve),
and the thick moderator band (MB) in the right ventricle.
110 A Practical Guide to 3D Ultrasound
Figure 11.33 The threshold and mix are adjusted further Figure 11.34 The direction of the internal light source is
in order to change the texture and appearance of the image. changed in order to reversely illuminate the heart.
The fetal chest is an area that has received much attention The two main areas of utility of volume sonography in the
with 3D sonography, especially with respect to fetal lung fetal chest are first, fetal lung development and the establish-
volume measurements. Pulmonary hypoplasia remains a ment of volume normograms, and second, utilizing the vari-
major source of fetal morbidity and mortality. Pulmonary ous 3D modes to enable more precise diagnoses in fetal lung
hypoplasia may be the result of several maternal and fetal abnormalities.
conditions, oligohydramnios caused by premature rupture of
membranes or renal disease, skeletal dysplasias, chylothorax
(Figure 12.1), pulmonary masses, and fetal diaphragmatic
hernia (Figure 12.2 and 12.3). With the availability of fetal Areas of Utility of Volume
endotracheal occlusion (FETO) for antenatal management Sonography in the Fetal Chest
of fetal diaphragmatic hernia, lung volume assessments 1. Lung development and establishing lung
become critical. Fetal lung volumes are calculated pre- and volume normograms
post-FETO for patient selection and for the determination of 2. Assessing lung abnormalities
procedural impact. This has led to several studies investigat-
ing the role of volume sonography in accurately quantifying
fetal lung volume.
Right
L
A AS
V
V Left
L VS
B C
Figure 12.1 A 3D volume of the fetal chest of a 20w5d fetus with chylothorax. (A) The volume is displayed in the multiplanar mode
using sepia. Note the small fetal lungs (L). (B) The same volume displayed using TUI at an interslice thickness of 3 mm and VCI at a slice
thickness of 3 mm, depicting the extent of the chylothorax. (C) A surface-rendered image of the heart and lungs facilitated by the acoustic
window created by the fluid filling the chest. V, ventricle; VS, ventricular septum; AS, atrial septum.
111
112 A Practical Guide to 3D Ultrasound
L
S
Table 12.1 Steps to Measuring Fetal Lung Volume in Congenital Diaphragmatic Hernia
Step 1: Obtain an axial section through the anterior fetal chest at the level of the four-chamber view
Step 2: Place the acquisition box around the entire chest, with an angle of acquisition of 55 degrees and a mid to high quality for the volume
Step 3: Acquire the volume and display it in the multiplanar mode (Figure 12.4)
Step 4: Select VOCAL and use manual trace at a rotational angle of 30 degrees and hit “next” (Figure 12.5)
Step 5: Point trace the right lung (Figure 12.6) and repeat this step in all six rotational planes
Step 6: Once the right lung has been traced in all six rotational planes, hit “done” and a 3D reconstruction of the lung appears with the volume
calculated (Figure 12.7)
Step 7: The final rendered volume may be displayed as a mesh and rotated along all three axes (Figure 12.8)
Clinical Applicability in the Fetal Chest 113
S
L
Figure 12.7 Once all six measurements are obtained, a 3D schematic of the compressed lung is generated and its volume is calculated:
8.429 cm2 in this case.
Volume Sonography in Fetal Lung Abnormalities malformation of the lung (CCAM) in fetuses with a hyper-
echogenic lung mass by identifying the feeding vessel. This
Another utility of volume sonography is in its role in is helpful in prenatal counseling and postnatal management
localizing and evaluating the lungs (Figure 12.9), further (Ruano et al. 2005b).
characterizing lung lesions and mapping out their extent,
involvement of adjacent structures, and their vasculature. A
study by Achiron et al. presented an overview of the various
modalities in volume sonography and addressed where to
use which modality to further enhance the diagnostic accu- Clinical Utility OF VOLUME
racy in cases of lung abnormalities (Achiron et al. 2008). SONOGRAPHY IN LUNG ABNORMALITIES
Another report by Ruano et al. on a case of a posterior 1. Localizing chest abnormalities
mediastinal lymphangioma concluded that 3D was helpful 2. Assessing lung abnormalities
in determining the precise location of the mass (Ruano et 3. Differentiating CCAM from pulmonary
al. 2008). Ruano et al. also investigated the role of 3D power sequestration
Doppler and found it to be critical in differentiating pul-
monary sequestration from congenital cystic adenomatoid
L L
Introduction in the late second and third trimesters. The main areas of rel-
evance are with respect to quantifying bowel echogenicity,
Gastrointestinal abnormalities tend to be identified in the characterizing abdominal wall defects (Figure 13.1 and 13.2),
late second and early third trimesters of pregnancy except assessing liver volume, and assessing abdominal vasculature,
in cases of abdominal wall defects or hyperechogenic bowel. with isolated reports on other gastrointestinal abnormalities
Similar to the genitourinary tract, the gastrointestinal tract (Figures 13.3–13.5).
contains several fluid-filled structures. As a consequence, the
role of the inversion mode becomes apparent, as does TUI,
enabling serial slices spanning the abdominal cavity and pel- Areas in the Gastrointestinal
vis allowing for the characteriztion and accurate identifica- Tract to be Assessed by
tion of the lesion under suspicion. Volume Sonography
1. Echogenic bowel
2. Abdominal wall defects
Clinical Utility 3. Liver volume
4. Abdominal vasculature
Most reports on describing the use of volume sonography in 5. Other areas in the gastrointestinal tract
evaluating the gastrointestinal tract are limited to case reports
Figure 13.1 A sagittal 3D volume of a 11w6d fetus with an omphalocele displayed using TUI at an
interslice thickness of 1.2 mm. The reference dot is placed in the fetal omphalocele and localizes it in all
the 2D planes.
117
118 A Practical Guide to 3D Ultrasound
CI
S
EB
S
B
Figure 13.7 An axial 3D volume of the abdomen of a 32w1d fetus displayed in the mul-
tiplanar mode. B: bladder; S: stomach.
S
B
Figure 13.8 VOCAL is now selected with a rotational Y axis bisecting the fetal abdomen.
B: bladder; S: stomach.
122 A Practical Guide to 3D Ultrasound
S
B
Figure 13.9 Manual trace with a rotational angle of 30 degrees is then selected and the
fetal liver is traced in six consecutive planes. B: bladder; S: stomach.
Figure 13.10 Once all six measurements are obtained, a 3D schematic of the liver is
generated and its volume calculated: 106.54 cm2 in this case. The final rendered schematic
may be rotated along any of the three axes.
Clinical Applicability in the Fetal Gastrointestinal Tract 123
One of the first studies on the use of 3D power Doppler for Ramón y Cajal et al. reported on the utility of 3D in differ-
the study of the fetal abdominal vasculature was by Chaoui entiating the duodenal and gastric cavities and visualizing
et al. where the study was able to differentiate the spleen the connecting pyloris in a case of duodenal artesia (Ramón
from the liver and confirm the presence of splenomegaly in a y Cajal et al. 2003). Yagel reported on a case of esophageal
case of cytomegalovirus infection (Chaoui et al. 2002). Paris atresia where 3D facilitated the diagnosis and visualization
et al. mapped out the anatomy of the portal sinus using 3D of the atretic portion of the esophageal pouch (Yagel 2005).
angiography (Paris et al. 2004). Subsequently, Loureiro et Ramon y Cajal et al. reported on visualization of fetal def-
al. utilized 3D power Doppler to study the vasculature of a ecation using 4D sonography (Ramón y Cajal et al. 2005).
congenital abdominal hemangioma and was able to display In cases of fetal ascites, the intra-abdominal fluid provides
the feeding vessel (Loureiro et al. 2008). Sammour et al. a window through which to obtain nice intra-abdominal
diagnosed prenatal volvulus using 3D Doppler, where the 3D images (Figure 13.11 and 13.12).
counterpart to the 2D “whirlpool sign” was described. This
was called the “barber pole” sign (Sammour et al. 2008).
PE
Figure 13.11 A 3D volume of 23w2d fetus with ascites displayed using the multiplanar
mode with VCI at a thickness of 2 mm. A: ascitis; B: bowel, L: liver; PE: pleural effusion.
124 A Practical Guide to 3D Ultrasound
Figure 13.12 The same volume from Figure 13.11 now displayed in TUI at an interslice thickness
of 2 mm and VCI at a slice thickness of 2 mm, showing the small echogenic bowel and the extent of the
ascites. It is possible to use VOCAL in this case to quantify the ascites for follow-up of the progression
with advancing gestation. A: ascitis, B: bowel.
125
126 A Practical Guide to 3D Ultrasound
A B
Figure 14.2 3D examination of the external genitalia. (A) A 3D volume of the external genitalia of
a 27w0d male fetus rendered using surface rendering. The scrotum and penis can be depicted with great
clarity. (B) The volume is now displayed using HDlive.
EG
A B
Figure 14.3 3D examination of ambiguous external fetal genitalia (EG). (A) A 3D volume of the exter-
nal genitalia of a 34w5d fetus displayed using surface rendering with HDlive. The 2D image in plane A
depicts the “tulip” sign described in hypospadius. The 3D surface-rendered image was highly suggestive
of swollen labia in a female fetus. (B) A close-up of the external genitalia. This fetus was a live born male
with hypospadias.
EG
A B
Figure 14.4 A 22w3d fetus with multiple anomalies. (A) A 3D volume of ambiguous external genitalia
(EG) is acquired and displayed using surface rendering. (B) The Volume is manipulated by adjusting the
size of the render box and rotating along the three axes. Surface rendering is used, depicting seemingly
female external genitalia. However, postmortem this was a male fetus with hypospadias and a bifid scrotum.
Clinical Applicability in the Fetal Genitourinary System 127
at 20–22 and 32–34 weeks in an attempt to further enhance Fetal Urine Production
the endometrial visualization. The VCI mode clarified the
distinction between the uterus and rectum (Jouannic et al. The amniotic fluid index may be measured in several ways,
2005). and the importance of quantifying the amniotic fluid lies in
its ability to indicate adequate fetal vascularization, in the
absence of fetal hypoxia, reflected by good urine production.
Utility of Volume Sonography in However, the amniotic fluid is not made up entirely of urine,
the Evaluation of Fetal Gender and there have been various attempts at quantifying the
1. Clarifying ambiguous genitalia amount of fetal urine production more accurately, an area in
2. Utilizing the mid-sagittal plane for first- which volume sonography has played a role. Lee et al. exam-
trimester sex determination ined 154 fetuses, between 24 and 40 weeks, and employed
3. Utilizing VCI for the clarification of the VOCAL in order to measure the fetal bladder volume two
endometrial stripe to three times within a 5–10 minute period. The mean fetal
bladder volume was plotted against the gestational age. This
may be an alternative method for quantifying the amniotic
fluid index, and it may aid in signaling fetal hypoxia (Lee
Renal Pelvis et al. 2007). Similarly, Yamamato et al. looked at fetal urine
production using VOCAL in 106 twin-to-twin-transfusion
Hydronephrosis (Figure 14.5) is a marker for chromosomal syndrome cases, pre- and post-laser, to determine how it cor-
aberrations and exists in a continuum of gradations. It may be related with umbilical venous volume flow. The conclusion
benign or it may signal underlying renal disease, from uret- was that urine production is a useful tool in assessing the
ropelvic junction obstruction in its varying degrees, to reflux. severity of twin-to-twin-transfusion syndrome (Yamamato et
Measuring the anteroposterior diameter of the renal pelvis al. 2007).
has been the gold standard, but with the advent of volume
sonography, the volume of the renal pelvis can now be mea-
sured. Duin et al. succeeded in measuring the volume of the
fetal renal pelvis in 15 fetuses and found it feasible and repro- Utility of Volume Sonography
ducible, but in need of comparison to the standard antero- in the Evaluation of Fetal
posterior measurement to determine its clinical utility (Duin Urine Production
et al. 2008). In addition, the inversion mode may be of great 1. Quantifying urine production
use in mapping out the entire pelvis and calyceal system in
cases of hydronephrosis (Table 14.1; Figures 14.6–14.8) and
in creating a true cast of the calyceal system.
*
*
*
Figure 14.6 A 3D volume of the left
kidney of a 31w4d fetus with hydrone-
phrosis (*). The volume is acquired with
an angle of acquisition of 55 degrees and
displayed in the three orthogonal planes.
H
C
Other Uses in the Genitourinary Tract al. used 4D sonography in a case of fetal lower urinary tract
obstruction as a guide to percutaneous cystoscopy, and this
Schild et al. reported on the use of 3D in a case of fetal meso- was the first fetal cystoscopy under 4D guidance (Ruano et al.
blastic nephroma that was initially diagnosed as a Wilms’ 2009). Volume sonography may also help in the evaluation of
tumor. The 3D imaging allowed volume calculation and a reli- the fetus with megacystis (Figures 14.9–14.11).
able estimation of the size of the mass as well as characteriza-
tion of the borders of the mass (Schild et al. 2000). Dulay et
al. reported on the use of 3D in a case of vesicorectal fistula in
cloacal dysgenesis. The 3D imaging was key in identifying the
Other Uses of Volume
bladder with the umbilical arteries, as demonstrated by color
Sonography in the Evaluation
Doppler, and in finding the connection between the bladder
of the Genitourinary Tract
and bowel by scrolling through the volume (Dulay et al. 2006).
Hsu et al. found 3D power Doppler helpful in localizing an 1. In the evaluation of tumors
aberrant renal artery arising from the iliac artery and feed- 2. In the evaluation of a fistula
ing the kidney’s inferior pole. Aberrant renal arteries may be a 3. In the evaluation of an ectopic kidney
normal variant and may arise from the aorta. In this case, com- 4. In guidance during fetal cystoscopy
bining 2D and 3D power angiography allowed the diagnosis of 5. In the evaluation of megacystis
a horseshoe kidney (Hsu et al. 2007). Most recently, Ruano et
130 A Practical Guide to 3D Ultrasound
H
C
Figure 14.11 This is the same volume from Figure 14.9. The volume is now displayed using TUI with
an interslice thickness of 3.8 mm and a VCI thickness of 2 mm, with the reference dot in the fetal bladder.
B: bladder; C: chest; H: head.
Limitations of Volume Sonography in the sonography, utilizing inversion mode as well as VOCAL,
Evaluation of the Genitourinary System aids in evaluating the fetal calyceal system in cases of hydro-
nephrosis, and may help in quantifying urine production.
The major limitation with volume sonography in the geni-
tourinary system is false diagnoses, especially in cases
of ambiguous genitalia. Therefore the examiner needs Practical Pearls
to carry out a meticulous evaluation, relying on internal
as well as external 2D findings, prior to announcing the
fetal gender to the family based solely on a 3D surface-
• In order to visualize the kidneys, OmniView
rendered image.
may be utilized commencing with an axial
plane in order to generate coronal or sagittal
views of the kidneys
Conclusion
• Inversion mode is most useful in mapping out
the fetal calyceal system
Volume sonography has several key roles in the evaluation of
• VCI is helpful in the evaluation of fetal
the fetal genitourinary system. Surface rendering aids in visu-
hydronephrosis
alizing the external genitalia; however, navigating through a
• Minimum and inversion modes are helpful in
volume, looking for other signs such as the tulip sign and the
the evaluation of the kidneys and bladder
distance between the bladder and rectum (Glanc et al. 2007),
provides more conclusive information. In addition, volume
15 3D Applications in Obstetrics
In addition to what has already been discussed, there are con- Volume sonography can be an added benefit in several areas,
stantly emerging studies pertaining to the various applica- including evaluation of placental masses, placental localiza-
tions of volume sonography in obstetrics. The focus of this tion for suspected placenta previa (Figure 15.1), and whenever
chapter is therefore on other clinical applications of 3D ultra- there may be retained products of conception (Figure 15.2).
sound in obstetrics. Volume sonography is also helpful in ascertaining the num-
ber of cord loops (Figure 15.3) or true knots in the cord
(Figure 15.4) whenever these abnormalities are suspected.
Other Applications of Volume
Sonography in Obstetrics
1. Placenta and cord
Role of Volume Sonography in the
2. Fetal weight estimation
Evaluation of the Placenta and Cord
3. Fetal behavior
4. Review of topographic anatomy 1. Placental masses
5. Intrapartum role 2. Placental localization
3. Retained products of conception
4. Nuchal cord
5. True knot in the cord
Clinical Utility
*
Cx
A B
Figure 15.1 A 12w6d intrauterine pregnancy with a suspected placenta previa. (A) Transvaginal evaluation reveals a central previa com-
pletely covering the internal cervical os (Cx). (B) A 3D transvaginal volume of the uterus is displayed utilizing TUI at an interslice distance
of 0.8 mm, further ascertaining the central location of the placenta previa (*).
131
132 A Practical Guide to 3D Ultrasound
* *
*
*
* *
*
*
*
A B
Figure 15.2 A 3D transvaginally acquired volume of a postpartum uterus with retained products of conception (*). (A) The volume is
displayed in the multiplanar mode, clearly depicting retained placental products. (B) Surface rendering is utilized to display the volume.
The threshold and mix are adjusted to highlight the retained placental products, which are often challenging to depict with conventional 2D
sonography.
Figure 15.3 A 3D volume of a suspected entangled cord at Figure 15.4 A 3D volume of a 27w3d intrauterine pregnancy
35w6d utilizing color Doppler. Glass-body mode is used, highlight- with a true knot in the cord. The volume is displayed in the 3D CFM
ing the vascular structures and clarifying the entangled cord. mode, which highlights the vascular structure, illustrating the knot
in the cord.
3D Applications in Obstetrics 133
Estimation of Fetal Weight approach on how to calculate fetal weight from the fetal thigh
is described in Table 15.1. In a recent study by Pagani et al.,
A novel application for volume sonography, which has been its use in fetal weight estimation in mothers with gestational
studied by Lee et al. (2001b, 2009), is the use of fetal arm diabetes mellitus was found to be of comparable sensitiv-
and leg volumes to assist in the accurate estimation of fetal ity but of superior specificity in fetal weight estimation at
weight. This application has been developed into a software 34w0d–36w6d when compared to the conventional Hadlock
program currently available on certain machines. A stepwise formula for predicting fetal macrosomia (Pagani et al. 2014).
A B
Figure 15.5 A 3D volume of a fetal thigh at 31w3d displayed in a single pane (plane of acquisition plane A) of the multiplanar mode. (A)
The original volume with the arrow pointing to the reference dot. (B) The reference dot (arrow) has now been moved to a central position
along the midpoint of the fetal femur.
Figure 15.7 Using the area trace, the circumference of the fetal thigh is encircled sequentially in each of the five
generated volumes.
Figure 15.8 Once all five tracings are complete, the system displays the tracings in a single view with an auto-
matically generated fractional limb volume from which the fetal weight is generated.
3D Applications in Obstetrics 135
Figure 15.10 A 3D surface-rendered image of a 21w5d fetus Figure 15.11 A 3D surface-rendered image of a 23w5d fetus
sucking his thumb. hiding its face behind both hands.
136 A Practical Guide to 3D Ultrasound
A B
Figure 15.13 A 3D surface-rendered volume of a 30w1d fetus with open eyes. Note artifact (*) generated by fetal movement. (A) The
volume is displayed in the multiplanar mode with surface rendering. (B) The volume is rendered with HDlive.
3D Applications in Obstetrics 137
The role of volume sonography in the review of topographic The role of volume sonography in assessing the position
anatomy has been assessed, and it was found to be useful of the fetal head during labor has been studied by several
in the evaluation of first trimester losses. For instance, in a experts, at the forefront of which is Pilu’s group, leading to
case of a missed abortion, 3D ultrasound identified the pres- the development of the SonoVCADlabor software to monitor
ence of conjoined twins, otherwise missed by conventional fetal head progression in the birth canal during labor (Ghi et
2D ultrasound, at a challenging early point in gestation where al. 2010). It has recently been shown that there is a good cor-
the patient had presented with fetal demise (Abu-Rustum and relation between 2D and 3D sonography in the evaluation of
Adra 2007) (Figure 15.14). In addition, a study by Bromley the head-to-symphysis distance (Youssef 2013).
et al. found it to be of benefit in the evaluation of fetuses pre-
senting with first trimester demise as it helped clarify various
external structural abnormalities that were otherwise missed Limitations of Volume Sonography in Obstetrics
by 2D ultrasound (Bromley et al. 2010).
The major limitation to utilizing these various applica-
tions of 3D ultrasound in obstetrics remains the steep
learning curve, in addition to added cost of some of the
software mentioned.
139
140 A Practical Guide to 3D Ultrasound
A B
C D
Figure 16.2 A transvaginal sonohysterography with saline infusion. (A) 2D sagittal image of
the fluid-filled endometrial cavity is obtained. (B) Volume of the uterus is now acquired and is
displayed in the three orthogonal planes. (C) Rotation along the X, Y, and Z axes has been carried
out, and the single pane has been chosen. Note the catheter tip (arrow). (D) The volume is now
displayed using TUI at an interslice distance of 1.5 mm, allowing for a more comprehensive evalu-
ation of the normal endometrial cavity.
Table 16.1 Steps to Utilizing the Z Technique to Obtain the Mid-Coronal View of the Uterus
Step 1: Obtain a 3D volume of the uterus starting from the sagittal plane (Figure 16.4)
Step 2: Display the volume in the multiplanar mode (Figure 16.5)
Step 3: Place the reference dot in the center of the endometrial stripe in plane A (Figure 16.6)
Step 4: Align the sagittal plane to depict the endometrial stripe as horizontally as possible in plane A by rotating along the Z axis (Figure 16.7)
Step 5: Select plane B and rotate along the Z axis in order to align the endometrial stripe horizontally (Figure 16.8)
Step 6: The mid-coronal plane will be automatically displayed in plane C and may be optimized by rotation along the Z axis (Figure 16.9)
Cx
Cx
Cx
Cx
E
E
Figure 16.7 Rotation along the Z axis
is then carried out in plane A to align the
endometrial stripe in as horizontal a lie as
possible. Cx: cervix; E: endometrium.
Cx
E
A B C
Figure 16.9 Coronal view of the uterus. (A,B,C) Plane C is selected and rotation along the Z axis is then carried out to
orient the endometrial cavity in its normal anatomical position. The image threshold, transparency, and color are adjusted to
optimize the depiction of the coronal view of the uterine cavity.
3D Applications in Gynecology 143
One of the greatest roles for volume sonography has been Volume sonography provides clarification of the characteris-
in assisted reproduction, particularly in tracking ovar- tics of all gynecological tumors to help differentiate benign
ian follicles. This has been facilitated through the use of from malignant tumors. By utilizing the various rendering
SonoAVC. Obtaining a 3D volume of an ovary and activat- techniques, it is possible to visualize hair within mature tera-
ing SonoAVC makes it possible to automatically color-code, tomas (Figure 16.10), excrescences (Figure 16.11), and obtain
count, and calculate the volume of all the follicles within 3D renderings to study complex vascularity. In addition, eval-
an ovary, thus facilitating optimal management of patients uating tubal pathology and differentiating tubal (Figure 16.12)
undergoing ovarian stimulation and properly timing oocyte from ovarian pathology (Figure 16.13) is greatly facilitated.
retrieval. The steps for using inversion on a cystic ovary and
SonoAVC to calculate follicular number and volume were
covered in Chapters 4 and 6 (Tables 4.2 and 6.3; Figure 4.12
and Figures 6.13–6.15).
*
*
A B
Figure 16.11 A transvaginal 3D volume of an ovarian tumor is obtained. (A) The volume is displayed in the multiplanar mode. (B) The
volume is rendered using surface rendering, depicting the solid nature of the mass with excrescences (*).
144 A Practical Guide to 3D Ultrasound
*
*
O
O
A C
Figure 16.13 A transvaginal 3D volume of the adnexa displayed using inversion mode,
depicting multiple follicles in a patient with hyperstimulation syndrome.
3D Applications in Gynecology 145
Sonohysterography
* *
*
A B C
Figure 16.15 A transvaginal 3D volume of the endometrial cavity from two patients displayed in the coronal view, illustrating a per-
fectly placed intrauterine device (IUD) (*). (A) Final surface-rendered coronal plane of patient 1. (B) Volume of patient 2 displayed in the
three orthogonal planes and rendered with the minimum mode. (C) Final rendered image of patient 2 using minimum mode where the color
settings have been adjusted, clearly displaying the proper placement and the shape of the Cu-T 380A IUD.
*
*
S
*
* S
* *
A B
Figure 16.17 Transvaginal coronal view of the endometrial cavity for the localization of an intrauter-
ine device (IUD) (*). (A) Utilizing the Z technique demonstrates a uterine septum with the IUD to the left
of the septum. (B) Employing TUI at an interslice thickness of 3.1 mm and VCI at a slice thickness of 3.4
mm generates a clear depiction of the endometrial cavity, the septum (S), and the location of the IUD.
Volume sonography requires time and dedication to develop Although CPT codes for 3D ultrasound have been intro-
the necessary skill and to employ the various 3D modalities duced, reimbursement remains minimal and there is a con-
available. However, 2D ultrasound remains the “gold stan- sensus among global organizations such as the American
dard,” where in experienced hands its use is sufficient to Institute of Ultrasound in Medicine (AIUM) (http://www.
arrive at the most complicated diagnoses. Because of this, aium.org), the Society for Maternal-Fetal Medicine (SMFM)
billing and third-party coverage for 3D ultrasound continue (http://www.smfm.org), and the American Congress of
to face major limitations. Although the practitioner may bill Obstetricians and Gynecologists (ACOG) (http://www.acog.
for a 3D sonographic examination, reimbursement, unless for org) in North America that unless medically indicated, there
specific indications, remains minimal. should be no billing for a 3D scan. The physician may still
choose to obtain 3D images for the patient at no additional
cost. However, for certain indications where there is suffi-
Coding cient evidence of the added benefits of 3D ultrasound, it may
be possible to bill using the 3D ultrasound-specific codes
Performing a 3D examination requires costly sonographic (Table 17.3) (APS Medical Billing 2013).
equipment in addition to a steep learning curve for the prac- There are many resources available pertaining to coding in
titioner. It also requires time allocation during the examina- obstetrics and gynecology, and recent comprehensive online
tion and additional time is required for off-line analysis after
completion of the examination. With limited reimbursement,
this is a major challenge hindering the widespread use of 3D
ultrasound in obstetrics and gynecology (Ob/Gyn). Table 17.2 Various CPT Codes in Obstetrical
Sonography
CPT 76801 Transabdominal first trimester (<14w0d) fetal and
maternal evaluation of a single or first gestation. Use
Indications for Potential CPT +76802 for each additional gestation
Reimbursement in 3D Sonography CPT 76805 Transabdominal fetal and maternal evaluation (>
14w0d) of a single or first gestation. Use CPT +76810
1. Skeletal abnormalities for each additional gestation
2. Facial anomalies CPT 76811 An indication-based examination not for routine use in
3. Uterine anomalies all pregnancies. To be used once per pregnancy. Use
CPT +76812 for each additional gestation
CPT 76813 Transabdominal or transvaginal evaluation with nuchal
translucency measurement for a single or first gestation.
Coding in Ob/Gyn Sonography Use CPT +76814 for each additional gestation
CPR 76815 Limited evaluation of the fetal heartbeat, placental
There are various codes that may be used in Ob/Gyn sonog- location, fetal position, and amniotic fluid index on 1 or
raphy. Tables 17.1 and 17.2 list the major codes with their more fetuses
requirements (GE Healthcare 2011; United Healthcare 2013; CPT 76816 If 76811 did not allow a full evaluation, a focused
AIUM 2014) for the United States. reassessment may be planned and code 76816 may be
used for the follow-up examination
CPT 76817 Transvaginal evaluation with image documentation
CPT 76820 Fetal and umbilical artery Doppler velocimetry
Table 17.1 Various CPT Codes in Gynecological
CPT 76821 Fetal middle cerebral artery velocimetry
Sonography CPT 76825 Echocardiography (2D) with or without M-mode
CPT 76856 Complete pelvic, nonobstetric, real-time examination recording
with image documentation CPT 76826 Follow up or repeat to CPT 76825
CPT 76857 Limited or follow-up pelvic, nonobstetric, real-time CPT 76827 Complete Doppler echocardiography
examination with image documentation (for instance, for CPT 76828 Follow up to CPT 76827
follicular monitoring)
147
148 A Practical Guide to 3D Ultrasound
resources are available through the AIUM and other organi- Conclusion
zations (GE Healthcare 2011; United Healthcare 2013; APS
Medical Billing 2013; AIUM 2014). Despite the role of 3D ultrasound in clarifying various fetal
structural defects and its role in the evaluation of the uterine
cavity, reimbursement for an examination that requires cost-
Table 17.3 Various CPT Codes in 3D Sonography lier machines, more operator skill, and more time allocation
CPT 76376 3D rendering with post-processing interpretation; remains the greatest challenge. The practitioner must acquire
however, not requiring post-processing on a separate the needed skills during daily practice and by attending
workstation structured hands-on workshops whenever possible, in addi-
CPT 76377 3D rendering with post-processing interpretation; tion to using off-line software to gain more skill in volume
however, requiring post-processing on a separate manipulation. Various global organizations, at the forefront
workstation of which is the AIUM, through such initiatives as Ultrasound
First (http://www.ultrasoundfirst.org), are raising awareness
as to the tremendous role of ultrasound in general as a first-
line imaging modality, and to 3D ultrasound in particular as
“Entertainment Ultrasound” an indispensible diagnostic tool in gynecology. Awareness
will lead to better utilization and provide further clinical evi-
At the conclusion of this guide on volume sonography, hav- dence, ultimately leading to better reimbursement. Volume
ing discussed all the basic aspects of the various techniques sonography is here to stay despite all the obstacles. It is time
and where and how to utilize them, there must be a brief clos- to confidently incorporate it into daily clinical practice as a
ing discussion on “entertainment ultrasound.” This nonmedi- complementary modality to properly performed 2D sonog-
cal use of ultrasound, also known as “keepsake” imaging, raphy, and to maximize its potential role as an invaluable
has tainted the image of volume sonography. As the practi- tool in helping the clinicians and families better appreciate
tioner commences on incorporating volume sonography into complicated fetal anomalies. This will facilitate planning
daily clinical practice, it is critical to maintain focus on the antepartum, intrapartum, and postpartum care. Caution must
key constituents of a thorough obstetrical evaluation without be exercised against its use for non-medical purposes. This
losing sight of what is important, by misusing resources for novel method, when properly utilized, enhances the physi-
the sake of “pretty” images and perhaps falsely reassuring cian–patient relationship as well as patient-fetal bonding,
patients about the health and well-being of their fetuses. while providing reassurance and valuable information as to
Several press releases and position statements have been the health and well-being of our future generations.
issued by leading professional organizations cautioning
against the nonmedical use of ultrasound, at the forefront of
which are the AIUM and ACOG (AIUM 2002, 2004, 2005a,
2005b, 2005c, 2012; ACOG 2004). In addition, an article by Practical Pearls
Greene et al. attests to the false reassurance resulting from
keepsake imaging and presents the case of a patient whose
fetus was affected by trisomy 18 with seven key sonographic
markers present, none of which were detected by the keep- • Even though reimbursement is limited, the
sake scanner. The conflicting findings between the “enter- practitioner should practice his 3D skills at
tainment” and the “medical” sonograms were confusing for every opportunity
the family and hindered their acceptance of the fetal con- • One must be very familiar with coding and
dition (Greene and Platt 2005). Nonetheless, the consensus the indications
is that 3D sonography may serve to enhance the physician- • Caution is warranted against the non-medical
patient relationship. Therefore it may be a consideration, after use of ultrasound
the performance of a thorough obstetrical scan, to provide the • If possible, after a proper obstetrical exami-
family with nice keepsake images at the physician’s office, nation, keep-sake images of the fetus help
time and fetal position permitting, at no additional cost to the enhance the patient–physician relationship as
family, but this should be in accordance with proper medi- well as patient–fetal bonding
cal practice, while enhancing physician–patient bonding and
ensuring patient satisfaction.
References
Abuhamad AZ. 2004. Automated multiplanar imaging a novel Allen LM, Silverman RK, Nosovitch JT, Lohnes TM, Williams
approach to ultrasonography. J Ultrasound Med 23:573–576. KD. 2008. Exploring 3-dimensional imaging techniques in
Abuhamad AZ. 2005. Standardization of 3-dimensional vol- the prenatal interrogation of cebocephaly. J Ultrasound Med
umes in obstetric sonography: a required step for training 27:983–988.
and automation. J Ultrasound Med 24:397–401. Anandakumar C, Nuruddin Badruddin M, Chua TM, Wong YC,
Abuhamad AZ. 2006. Clinical implications of the echo Chia D. 2002. First-trimester prenatal diagnosis of ompha-
enhancement artifact in volume sonography of the uterus. J locele using three-dimensional ultrasonography. Ultrasound
Ultrasound Med 25:1431–1435. Obstet Gynecol 20:635–636.
Abuhamad AZ, Singleton S, Zhao Y, Bocca S. 2006. The Z tech- Antsaklis A, Daskalakis G, Theodora M, Hiridis P, Komita O,
nique: an easy approach to the display of the midcoronal Blanas K, Anastaskis A. 2011. Assessment of nuchal translu-
plane of the uterus in volume sonography. J Ultrasound Med cency thickness and the fetal anatomy in the first trimester of
25:607–612. pregnancy by two- and three-dimensional ultrasonography: a
Abuhamad AZ, Falkensammer P, Zhao Y. 2007. Automated pilot study. J Perinatal Med 39:185–193.
sonography: defining the spatial relationships of standard APS Medical Billing. 2013. 3D Reconstruction. www.apsmed-
diagnostic fetal cardiac planes in the second trimester of bill.com/newsletters/2013-02/3d-reconstruction.
pregnancy. J Ultrasound Med 26:501–507. Bahlmann F. 2000. Three-dimensional color power angiogra-
Abu-Rustum, RS. NIPT: A Matter of Critical Timing. Prenatal phy of an aneurysm of the vein of Galen. Ultrasound Obstet
Perspectives 2014; 2(2):5-6. Gynecol 15:341.
Abu-Rustum RS, Adra AM. 2007. Three-dimensional sono- Bahmaie A, Hughes SW, Clark T, Milner A, Saunders J, Tilling
graphic diagnosis of conjoined twins with fetal death in the K, Maxwell DJ. 2000. Serial fetal lung volume measure-
first trimester. J. Ultrasound Med 27:1662–1663. ment using three-dimensional ultrasound. Ultrasound Obstet
Abu-Rustum RS, Chaaban M. 2009. Is 3-dimensional sonogra- Gynecol 16:154–158.
phy useful in the prenatal diagnosis of ambiguous genitalia? Bault JP. 2006.Visualization of the fetal optic chiasma using
J Ultrasound Med 28:95–97. three-dimensional ultrasound imaging. Ultrasound Obstet
Abu-Rustum RS, Ziade MF, Abu-Rustum SE. 2012. Defining Gynecol. 28:862–864.
the spatial relationships between 8 anatomic planes in the Benacerraf BR, Spiro R, Mitchell AG. 2000. Using three-
11+6–13+6 week fetus. Prenat Diagn 32:875-882. dimensional ultrasound to detect craniosynostosis in a
Abu-Rustum RS, Frangieh A, Fahed R, Soutou B, Abdelahad A. fetus with Pfeiffer syndrome. Ultrasound Obstet Gynecol
2013. Limitations of 3-dimensional sonography in the prena- 16:391–394.
tal evaluation of a skin denudation syndrome. J Ultrasound Benacerraf BR, Benson CB, Abuhamad AZ, Copel JA,
Med 32:1301–1303. Abramowicz JS, DeVore GR, Doubilet PM, Lee W, Lev-
Achiron R, Gindes L, Zalel Y, Lipitz S, Weisz B. 2008. Three- and Toaff AS, Merz E, Nelson TR, O’Neill MJ, Parsons AK,
four-dimensional ultrasound: new methods for evaluating fetal Platt LD, Pretorius DH, Timor-Tritsch IE. 2005. Three-
thoracic anomalies. Ultrasound Obstet Gynecol 32:36–43. and 4-dimensional ultrasound in obstetrics and gynecol-
ACOG Committee Opinion. 2004. Nonmedical use of obstetri- ogy. Proceedings of the American Institute of Ultrasound
cal sonography. Number 297. in Medicine Consensus Conference. J Ulrasound Med
AIUM Press Release. 2002. AIUM Opposes Use of Ultrasound 24:1587–1597.
for Entertainment. www.aium.org/press/viewRelease. Benacerraf BR, Sadow PM, Barnewolt CE, Estroff JA, Benson
aspx?id=61 C. 2006. Cleft of the secondary palate without cleft lip diag-
AIUM Press Release. 2004. The AIUM Reaffirms Its Opposition nosed with three-dimensional ultrasound and magnetic reso-
to Entertainment Ultrasound. www.aium.org/press/viewRe- nance imaging in a fetus with Fryns’ syndrome. Ultrasound
lease.aspx?id = 66 Obstet Gynecol 27:566–570.
AIUM Press Release. 2005a. Beyond Tom Cruise—The Bigger Benacerraf BR. 2008. Ultrasound of Fetal Syndromes. Second
Ultrasound Picture. www.aium.org/press/viewRelease. Edition. London: Churchill Livingstone.
aspx?id = 85 Benavides-Serralde A, Hernández-Andrade E, Fernández-
AIUM Press Release. 2005b. The AIUM Releases New Delgado J, Plasencia W, Scheier M, Crispi F, Figueras F,
Statement Regarding Keepsake Imaging. www.aium.org/ Nicolaides KH, Gratacós E. 2009. Three-dimensional sono-
press/viewRelease.aspx?id = 102 graphic calculation of the volume of intracranial structures
AIUM Press Release. 2005c. AIUM Discourages the Sale and in growth-restricted and appropriate-for-gestational age
Use of Ultrasound Equipment for Personal Use in the Home. fetuses. Ultrasound Obstet Gynecol 33:530–537.
www.aium.org/press/viewRelease.aspx?id = 114 Benoit B. 1999. Three-dimensional ultrasonography of congeni-
AIUM Press Release. 2012. Keepsake Fetal Imaging. Approved tal ichthyosis. Ultrasound Obstet Gynecol 13:380.
April 1, 2012. Benoit B, Chaoui R. 2005. Three-dimensional ultrasound with
AIUM 76811 Task Force. 2014. Consensus report on the detailed maximal mode rendering: a novel technique for the diagno-
fetal anatomical ultrasound examination: indications, com- sis of bilateral or unilateral absence or hypoplasia of nasal
ponents and qualifications. J Ultrasound Med 33:189–195. bones in second-trimester screening for Down syndrome.
Allen LM, Maestri MJ. 2008. Three-dimensional sonographic Ultrasound Obstet Gynecol 25:19–24.
findings associated with ectrodactyly–ectodermal dysplasia–
clefting syndrome. J Ultrasound Med 27:149–154.
149
150 A Practical Guide to 3D Ultrasound
Bharudi M, Fong K, Toi A, Tomlinson G, Okun N. 2010. Fetal Chaoui R, Hoffmann J, Heling KS. 2004. Three-dimensional
anatomic survey using three-dimensional ultrasound in con- (3D) and 4D color Doppler fetal echocardiography using
junction with first-trimester nuchal translucency screening. spatio-temporal image correlation (STIC). Ultrasound
Prenat Diagn 30:267–273. Obstet Gynecol 23:535–545.
Blaas HG, Eik-Nes SH, Berg TKS, Olstad BAB. 1995. Three- Chaoui R, Levaillant JM, Benoit B, Faro C, Wegrzyn P,
dimensional imaging of the brain cavities in human embryos. Nicolaides KH. 2005. Three-dimensional sonographic
Ultrasound Obstet Gynecol 5:228–232. description of abnormal metopic suture in second- and third-
Blaas HGK, Eik-Nes SH, Isaksen CV. 2000a.The detection of trimester fetuses. Ultrasound Obstet Gynecol 26:761–764.
spina bifida before 10 gestational weeks using two- and Correa FF, Lara C, Bellver J, Remohí J, Pellicer A, Serra
three-dimensional ultrasound. Ultrasound Obstet Gynecol V. 2006. Examination of the fetal brain by transabdomi-
16:25–29. nal three-dimensional ultrasound: potential for routine
Blaas HGK, Eik-Nes SH, Vainio T, Vogt Isaksen C. 2000b. neurosonographic studies. Ultrasound Obstet Gynecol
Alobar holoprosencephaly at 9 weeks gestational age visual- 27:503–508.
ized by two- and three-dimensional ultrasound. Ultrasound Dagklis T, Borenstein M, Peralta CFA, Faro C, Nicolaides KH.
Obstet Gynecol 15:62–65. 2006. Three-dimensional evaluation of mid-facial hypopla-
Blaicher W, Lee A, Deutinger J, Bernaschek G. 2001. sia in fetuses with trisomy 21 at 11 + 0 to 13 + 6 weeks of
Sirenomelia: early prenatal diagnosis with combined two- gestation. Ultrasound Obstet Gynecol 28:261–265.
and three-dimensional sonography. Ultrasound Obstet Devonald KJ, Ellwood DA, Griffiths KA, Kossoff G, Gill RW,
Gynecol 17:542–543. Kadi AP, Nash DM, Warren PS, Davis W, Picker R. 1995.
Bocca SM, Oehninger S, Stadtmauer L, Agard J, Duran EH, Volume imaging: three-dimenional appreciation of the fetal
Sarhan A, Horton S, Abuhamad AZ. 2012. A study of the head and face. J Ultrasound Med 14:919–925.
cost, accuracy, and benefits of 3-dimensional sonography DeVore GR, Falkensammer P, Sklansky MS, Platt LD. 2003.
compared with hysterosalpingography in women with uter- Spatio-temporal image correlation (STIC): new technology
ine abnormalities. J Ultrasound Med 31:81–85. for evaluation of the fetal heart. Ultrasound Obstet Gynecol
Bocca SM, Abuhamad AZ. 2013. Use of 3-dimensional sonog- 22:380–387.
raphy to assess uterine anomalies. J Ultrasound Med 32:1–6. DeVore GR, Polanco B, Sklansky MS, Platt LD. 2004. The
Bongain A, Benoit B, Ejnes L, Lambert JC, Gillet JY. 2002. “spin” technique: a new method for examination of the
Harlequin fetus: three-dimensional sonographic findings fetal outflow tracts using three-dimensional ultrasound.
and new diagnostic approach. Ultrasound Obstet Gynecol Ultrasound Obstet Gynecol 24:72–82.
20:82–85. Dikkeboom CM, Roelfsema NM, van Adrichem LNA,
Bonilla-Musoles F, Raga F, Villalobos A, Blanes J, Osborne NG. Wladimiroff JW. 2004. The role of three-dimensional ultra-
1998. First-trimester neck abnormalities: three-dimensional sound in visualizing the fetal cranial sutures and fontanels
evaluation. J Ultrasound Med 17:419–425. during the second half of pregnancy. Ultrasound Obstet
Bonilla-Musoles F, Machado LE, Bailão LA, Osborne NG, Gynecol 24:412–416.
Raga F. 2001. Abdominal wall defects two- versus three- Duin LK, Willekes C, Vossen M, Beckers M, Offermans J,
dimensional ultrasonographic diagnosis. J Ultrasound Med Nijhuis JG. 2008. Reproducibility of fetal renal pelvis vol-
20:379–389. ume measurement using three-dimensional ultrasound.
Bonilia-Musoles F, Machado LE, Raga F, Osborne NG, Bonilla Ultrasound Obstetrics Gynecol 31:657–661.
Jr F. 2002. Prenatal diagnosis of sacrococcygeal teratomas Dulay AT, Schwartz N, Laser A, Greco MA, Monteagudo A,
by two- and three-dimensional ultrasound. Ultrasound Timor-Tritsch IE. 2006. Two- and 3-dimensional sono-
Obstet Gynecol 19:200–205. graphic diagnosis of a vesicorectal fistula in cloacal dysgen-
Borrell A, Santolaya-Forgas J, Horbaczewski C, Henry R, Dunn- esis sequence. J Ultrasound Med 25:1489–1494.
Albanese L, Robinson JN. 2011. Is the starting section for Espinoza J, Lee W, Comstock C, Romero R, Yeo L, Rizzo G,
3D volume acquisition in the first trimester relevant in the Paladini D, Viñals F, Achiron R, Gindes L, Abuhamad A,
post hoc analysis of aneuploidy screening markers and fetal Sinkovskaya E, Russell E, Yagel S. 2010. Collaborative
anatomy? Prenat Diagn 31:1305–1310. study on 4-dimensional echocardiography for the diagnosis
Bromley B, Shipp TD, Benacerraf BR. 2010. Structural anoma- of fetal heart defects: the COFEHD study. J Ultrasound Med
lies in early embryonic death: a 3-dimensional pictorial 29:1573–1580.
essay. J Ultrasound Med 29:445–453. Faro C, Benoit B, Wegrzyn P, Chaoui R, Nicolaides KH. 2005.
Budorick NE, Pretorius DH, Johnson DD, Nelson TR, Tartar Three-dimensional sonographic description of the fetal fron-
MK, Lou KV. 1998. Three-dimensional ultrasonography tal bones and metopic suture. Ultrasound Obstet Gynecol
of the fetal distal lower extremity: normal and abnormal. J 26:618–621.
Ultrasound Med 17:649–660. Fauchon DEV, Benzie RJ, Wye DA, Cairns DR. 2008. What
Cafici D, Iglesias A. 2002. Prenatal diagnosis of severe hypo- information on fetal anatomy can be provided by a single
spadias with two- and three-dimensional sonography. J first-trimester transabdominal three-dimensional sweep?
Ultrasound Med 21:1423–1426. Ultrasound Obstet Gynecol 31:266–270.
Campbell S, Lees CC. 2003. The three-dimensional reverse face Faure JM, Captier G, Bäumler M, Boulot P. 2007. Sonographic
(3D RF) view for the diagnosis of cleft palate. Ultrasound assessment of normal fetal palate using three-dimensional
Obstet Gynecol 22:552–554. imaging: a new technique. Ultrasound Obstet Gynecol
Campbell S, Lees C, Moscoso G, Hall P. 2005. Ultrasound ante- 29:159–165.
natal diagnosis of cleft palate by a new technique: the 3D Faure JM, Bäumler M, Boulot P, Bigorre M, Captier G. 2008.
“reverse face” view. Ultrasound Obstet Gynecol 25:12–18. Prenatal assessment of the normal fetal soft palate by three-
Chaoui R, Zodan-Marin T, Wisser J. 2002. Marked splenomeg- dimensional ultrasound examination: is there an objective
aly in fetal cytomegalovirus infection: detection supported technique? Ultrasound Obstet Gynecol 31:652–656.
by three-dimensional power Doppler ultrasound. Ultrasound Gagel K, Heling KS, Kalache KD, Chaoui R. 2003. Prenatal
Obstet Gynecol 20:299–302. diagnosis of an intracranial arteriovenous fistula in the poste-
rior fossa on the basis of color and three-dimensional power
Doppler ultrasonography. J Ultrasound Med 22:1399–1403.
References 151
GE Healthcare. 2011. Reimbursement information for diag- Hull AD, Pretorius DH, Lev-Toaff A, Budorick NE, Salerno CC,
nostic ultrasound procedures completed by obstetricians. Johnson MM, James G, Nelson TR. 2000. Artifacts and the
www3.gehealthcare.com/en/Products/Categories/~/media/ visualization of fetal distal extremities using three-dimen-
Downloads/us/Product/Product-Categories/Ultrasound/ sional ultrasound. Ultrasound Obstet Gynecol 16:341–344.
GEHealthcare-Brochure_Reimbursement-Info-Obstetricians. Hunter S, Heads A, Wyllie J, Robson S. 2000. Prenatal diagnosis
pdf of congenital heart disease in the northern region of England:
Gerards FA, Engels MAJ, Barkhof F, van den Dungen FAM, benefits of a training programme for obstetric ultrasonograp-
Vermeulen RJ, van Vugt JMG. 2003. Prenatal diagnosis ghers. Heart 84:294–298.
of aneurysms of the vein of Galen (vena magna cerebri) Izquierdo MT, Bahamonde A, Domene J. 2009. Prenatal diagno-
with conventional sonography, three-dimensional sonogra- sis of a complete cleft sternum with 3-dimensional sonogra-
phy, and magnetic resonance imaging. Report of 2 cases. J phy. J Ultrasound Med 28:379–383.
Ultrasound Med 22:1363–1368. Johnson JM, Benoit B, Pierre-Louis J, Keating S, Chitayat D.
Gerards FA, Engels MAJ, Twisk JWR, van Vugt JMG. 2006. 2005. Early prenatal diagnosis of oculoauriculofrontona-
Normal fetal lung volume measured with three-dimensional sal syndrome by three-dimensional ultrasound. Ultrasound
ultrasound. Ultrasound Obstet Gynecol 27:134–144. Obstet Gynecol 25:184–186.
Gerards FA, Twisk JWR, Bakker M, Barkhof F, van Vugt JMG. Jouannic JM, Rosenblatt J, Demaria F, Jacobs R, Aubry MC,
2007. Fetal lung volume: three-dimensional ultrasonography Benifla JL. 2005. Contribution of three-dimensional volume
compared with magnetic resonance imaging. Ultrasound contrast imaging to the sonographic assessment of the fetal
Obstet Gynecol 29:533–536. uterus. Ultrasound Obstet Gynecol 26:567–570.
Ghi T, Contro E, Farina A, Nobile M, Pilu G. 2010. Three- Kalache KD, Espinoza J, Chaiworapongsa T, Londono J,
dimensional ultrasound in monitoring progression of Schoen ML, Treadwell MC, Lee W, Romero R. 2003. Three-
labor: a reproducibility study. Ultrasound Obstet Gynecol dimensional ultrasound fetal lung volume measurement: a
36:500–506. systematic study comparing the multiplanar method with the
Gindes L, Benoit B, Pretorius DH, Achiron R. 2008. Abnormal rotational (VOCAL) technique. Ultrasound Obstet Gynecol
number of fetal ribs on 3-dimensional ultrasonography asso- 21:111–118.
ciated anomalies and outcomes in 75 fetuses. J Ultrasound Khandelwal M, Silva J, Chan L, Reece EA. 1999. Three-
Med 27:1263–1271. dimensional ultrasonographic technology to assess and com-
Gindes L, Hegesh J, Weisz B, Gilboa Y, Achiron R. 2009. Three pare echodensity of fetal bowel, bone, and liver in the second
and four dimensional ultrasound: a novel method for evaluat- trimester of pregnancy. J Ultrasound Med 18:691–695.
ing fetal cardiac anomalies. Prenat Diagn 29:645–653. Kim MS, Jeanty P, Turner C, Benoit B. 2008. Three-dimensional
Glanc P, Umranikar S, Koff D, Tomlinson G, Chitayat D. 2007. sonographic evaluations of embryonic brain development. J
Fetal sex assignment by sonographic evaluation of the pelvic Ultrasound Med 27:119–124.
organs in the second and third trimesters of pregnancy. J Krakow D, Santulli T, Platt LD. 2001. Use of three-dimensional
Ultrasound Med 26:563-569. ultrasonography in differentiating craniosynostosis from
Greene N, Platt LD. 2005. Nonmedical use of ultrasound: greater severe fetal molding. J Ultrasound Med 20:427–431.
harm than good? J Ultrasound Med 2:123–125. Krakow D, Williams III J, Poehl M, Rimoin DL, Platt LD. 2003.
Hamill N, Yeo L, Romero R, Hassan SS, Myers SA, Mittal Use of three-dimensional ultrasound imaging in the diagno-
P, Kusanovic JP, Balasubramaniam M, Chaiworapongsa sis of prenatal-onset skeletal dysplasias. Ultrasound Obstet
T, Vaisbuch E, Espinoza J, Gotsch F, Goncalves LF, Lee Gynecol 21:467–472.
W. 2011. Fetal cardiac ventricular volume, cardiac out- Kuno A, Hayashi Y, Akiyama M, Yamashiro C, Tanaka H,
put, and ejection fraction determined with 4-dimensional Yanagihara T, Hata T. 2002. Three-dimensional sonographic
ultrasound using spatiotemporal image correlation and vir- measurement of liver volume in the small-for-gestational-
tual organ computer-aided analysis. Am J Obstet Gynecol age fetus. J Ultrasound Med 21:361–366.
205:76.e1–10. Kurjak A, Abo-Yaqoub S, Stanojevic M, Basgul Yigiter A, Vasilj
Hata T, Aoki S, Manabe A, Hata K, Miyazaki K. 1998a. O, Lebit D, Naim Shaddad A, Badreldeen A, Nese Kavak Z,
Visualization of fetal genitalia by three-dimensional ultra- Miskovic B, Vladareanu R, Spalldi Barisic L, Azumendi G,
sonography in the second and third trimesters. J Ultrasound Younis M, Pooh RK, Salihagic Kadic A. 2010. The potential
Med 17:137–139. of 4D sonography in the assessment of fetal neurobehavior—
Hata T, Aoki S, Akiyama M, Yanagihara T, Miyazaki K. 1998b. multicentric study in high-risk pregnancies. J Perinat Med
Three-dimensional ultrasonographic assessment of fetal 38:77–82.
hands and feet. Ultrasound Obstet Gynecol 12:235–239. Laudy JAM, Janssen MMM, Struyk PC, Stijnen T, Wallenburg
Heling KS, Chaoui R, Bollmann R. 2000. Prenatal diagnosis of HCS, Wladimiroff JW. 1998. Fetal liver volume measure-
an aneurysm of the vein of Galen with three-dimensional ment by three-dimensional ultrasonography: a preliminary
color power angiography. Ultrasound Obstet Gynecol study. Ultrasound Obstet Gynecol 12:93–96.
15:333–336. Lee A, Kratochwil A, Deutinger J, Bernaschek G. 1995.
Hoffman JIE, Christianson R. 1978. Congenital heart disease Three-dimensional ultrasound in diagnosing phocomelia.
in a cohort of 19502 births with long-term follow-up. Am J Ultrasound Obstet Gynecol 5:238–240.
Cardiol 42:641–647. Lee SM, Park SK, Shim SS, Jun JK, Park JS, Syn HC. 2007.
Hsu CY, Chen CP, Lin CJ. 2007. An aberrant renal artery aris- Measurement of fetal urine production by three-dimensional
ing from the iliac artery imaged by three-dimensional power ultrasonography in normal pregnancy. Ultrasound Obstet
Doppler ultrasonography: a sign of fetal horseshoe kidney. Gynecol 30:281–286.
Ultrasound Obstet Gynecol 29:358–359. Lee TH, Shih JC, Peng SSF, Lee CN, Shyu MK, Hsieh FJ. 2000.
Hsu TY, Hsu JJ, Chang SY, Chang MS. 2002. Prenatal three- Prenatal depiction of angioarchitecture of an aneurysm of
dimensional sonographic images associated with Treacher the vein of Galen with three-dimensional color power angi-
Collins syndrome. Ultrasound Obstet Gynecol 19:413–414. ography. Ultrasound Obstet Gynecol 15:337–340.
152 A Practical Guide to 3D Ultrasound
Lee W, Blanckaert K, Bronsteen RA, Huang R, Romero R. Merz E, Miric-Tesanic D, Bahlmann F, Sedlaczek H. 1999.
2001a. Fetal iliac angle measurements by three-dimensional Prenatal diagnosis of fetal ambiguous gender using three-
sonography. Ultrasound Obstet Gynecol 18:150–154. dimensional sonography. Ultrasound Obstet Gynecol
Lee W, Deter RL, Ebersole JD, Huang R, Blanckaert K, Romero 13:217–219.
R. 2001b. Birth weight prediction by three-dimensional Michailidis GD, Papageorgiou P, Economides D. 2002.
ultrasonography fractional limb volume. J Ultrasound Med Assessment of fetal anatomy in the first trimester using two-
20:1283–1292. and three-dimensional ultrasound. Br J Radiol 75:215–219.
Lee W, Chaiworapongsa T, Romero R, Williams R, McNie B, Mittal P, Gonçalves LF, Kusanovic JP, Espinoza J, Lee W, Nien
Johnson A, Treadwell M, Comstock CH. 2002a. A diagnostic JK, Eleazar Soto E, Romero R. 2007. Objective evaluation of
approach for the evaluation of spina bifida by three-dimen- Sylvian fissure development by multiplanar 3-dimensional
sional ultrasonography. J Ultrasound Med 21:619–626. ultrasonography. J Ultrasound Med 26:347–353.
Lee W, McNie B, Chaiworapongsa T, Conoscenti G, Kalache Moeglin D, Benoit B. 2001. Three-dimensional sonographic
KD, Vettraino IM, Romero R, Comstock CH. 2002b. Three- aspects in the antenatal diagnosis of achondroplasia.
dimensional ultrasonographic presentation of micrognathia. Ultrasound Obstet Gynecol 18:81–83.
J Ultrasound Med 21:775–781. Moeglin D, Talmant C, Duyme M, Lopez AC. 2005. Fetal lung
Lee W, Deter RL, McNie B, Gonçalves LF, Espinoza J, volumetry using two- and three-dimensional ultrasound.
Chaiworapongsa T, Romero R. 2004. Individualized growth Ultrasound Obstet Gynecol 25:119–127.
assessment of fetal soft tissue using fractional thigh volume. Molina FS, Faro C, Sotiriadis A, Dagklis T, Nicolaides KH. 2008.
Ultrasound Obstet Gynecol 24:766–774. Heart stroke volume and cardiac output by four-dimensional
Lee W, Balasubramaniam M, Deter RL, Hassan SS, Gotsch F, ultrasound in normal fetuses. Ultrasound Obstet Gynecol
Kusanovic JP, Gonçalves LF, Romero R. 2009. Fractional 32:181–187.
limb volume—a soft tissue parameter of fetal body composi- Monteagudo A, Mayberry P, Rebarber A, Paidas M, Timor-
tion: validation, technical considerations and normal ranges Tritsch IE. 2002. Sirenomelia sequence first-trimester diag-
during pregnancy. Ultrasound Obstet Gynecol 33:427–440. nosis with both two- and three-dimensional sonography. J
Levaillant JM, Mabille M. 2005. Fetal sphenoid bone: imaging Ultrasound Med 21:915–920.
using three-dimensional ultrasound and computed tomogra- Muench MV, Zheng M, Bilica PM, Canterino JC. 2008.
phy. Ultrasound Obstet Gynecol 31:229–231. Prenatal diagnosis of a fetal epidural hematoma using 2- and
Lev-Toaff AS, Ozhan S, Pretorius D, Bega G, Kurtz AB, 3-dimensional sonography and magnetic resonance imaging.
Kuhlman K. 2000. Three-dimensional multiplanar ultra- J Ultrasound Med 27:1369–1373.
sound for fetal gender assignment: value of the mid-sagittal Nath CA, Oyelese Y, Yeo L, Chavez M, Kontopoulos EV,
plane. Ultrasound Obstet Gynecol 16:345–350. Giannina G, Smulian JC, Vintzileos AM. 2005. Three-
Lin HH, Liang RI, Chang FM, Chang CH, Yu CH, Yang HB. dimensional sonography in the evaluation and management
1998. Prenatal diagnosis of otocephaly using two-dimen- of fetal goiter. Ultrasound Obstet Gynecol 25:312–314.
sional and three-dimensional ultrasonography. Ultrasound Naylor CS, Carlson DE, Santulli, Jr, T, Platt, LD. 2001. Use of
Obstet Gynecol 11:361–363. three-dimensional ultrasonography for prenatal diagnosis of
Loureiro T, Cunha M, Jesus JM, Beires J, Montenegro N. ambiguous genitalia. J Ultrasound Med 20:1365–1367.
2008. Congenital abdominal hemangioma: three-dimen- Nelson TR, Pretorius DH, Hull A, Riccabona M, Sklansky MS,
sional power Doppler imaging and volume acquisition in James G. 2000. Sources and impact of artifacts on clinical
the assessment of tumor vasculature. Ultrasound Obstet three-dimensional ultrasound imaging. Ultrasound Obstet
Gynecol 31:593–596. Gynecol 16:374–383.
Malinger G, Lerman-Sagie T, Viñals F. 2006. Three-dimensional Osada H, Iitsuka Y, Masuda K, Sakamoto R, Kaku K, Seki K,
sagittal reconstruction of the corpus callosum: fact or arti- Sekiya S. 2002. Application of lung volume measurement by
fact? Ultrasound Obstet Gynecol 28:742–743. three-dimensional ultrasonography for clinical assessment
Martínez Ten P, Pérez Pedregosa J, Santacruz B, Adiego B, of fetal lung development. J Ultrasound Med 21:841–847.
Barrón E, Sepúlveda W. 2009. Three-dimensional ultrasound Pagani G, Palai N, Zatti S, Fratelli N, Prefumo F, Frusca T. 2014.
diagnosis of cleft palate: “reverse face,” “flipped face” or Fetal weight estimation in gestational diabetic pregnancies:
“oblique face”—which method is best? Ultrasound Obstet comparison between conventional and three-dimensional
Gynecol 33:399–406. fractional thigh volume methods using gestation-adjusted
Matsumi H, Kozuma S, Baba K, Kobayashi K, Yoshikawa H, projection. Ultrasound Obstet Gynecol 43:72–76.
Okai T, Taketani Y. 1996. Three-dimensional ultrasound is Paladini D, Vassallo M, Sglavo G, Lapadula C, Longo M, Nappi
useful in diagnosing the fetus with abdominal wall defect. C. 2005. Cavernous lymphangioma of the face and neck: pre-
Ultrasound Obstet Gynecol 8:356–358. natal diagnosis by three-dimensional ultrasound. Ultrasound
McGahan MC, Ramos GA, Landry C, Wolfson T, Sowell BB, Obstet Gynecol 26:300–302.
D’Agostini D, Patino C, Nelson TR, Pretorius DH. 2008. Paladini D, Volpe P. 2006. Posterior fossa and vermian mor-
Multislice display of the fetal face using 3-dimensional ultra- phometry in the characterization of fetal cerebellar abnor-
sonography. J Ultrasound Med 27:1573–1581. malities: a prospective three-dimensional ultrasound study.
Merhi ZO, Haberman S, Roberts J, Gretta Sobol-Benin G. 2005. Ultrasound Obstet Gynecol 27:482–489.
Prenatal diagnosis of palatal teratoma by 3-dimensional Paladini D, Sglavo G, Penner I, Pastore G, Nappi C. 2007.
sonography and color Doppler imaging. J Ultrasound Med Fetuses with Down syndrome have an enlarged anterior
24:1317–1320. fontanelle in the second trimester of pregnancy. Ultrasound
Merz E, Weber G, Bahlmann F, Miric-Tesanic D. 1997. Obstet Gynecol 30:824–829.
Application of transvaginal and abdominal three-dimen- Paladini D, Vassallo M, Sglavo G, Pastore G, Lapadula C, Nappi
sional ultrasound for the detection or exclusion of mal- C. 2008a. Normal and abnormal development of the fetal
formations of the fetal face. Ultrasound Obstet Gynecol anterior fontanelle: a three-dimensional ultrasound study.
9:237–243. Ultrasound Obstet Gynecol 32:755–761.
Merz E. 1998. Three dimensional ultrasound—a require-
ment for prenatal diagnosis? Ultrasound Obstet Gynecol
12:225–226.
References 153
Paladini D, Sglavo G, Greco E, Nappi C. 2008b. Cardiac screen- Roelfsema NM, Hop HCJ, van Adrichem LNA, Wladimiroff
ing by STIC: can sonologists performing the 20-week anom- JW. 2007a. Craniofacial variability index in utero: a three-
aly scan pick up outflow tract abnormalities by scrolling dimensional ultrasound study. Ultrasound Obstet Gynecol
the A-plane of STIC volumes? Ultrasound Obstet Gynecol 29:258–264.
32:865–870. Roelfsema NM, Hop WCJ, van Adrichem LNA, Wladimiroff
Paris L, Cabaret AS, Grall JY. 2004. Three-dimensional imag- JW. 2007b. Craniofacial variability index determined by
ing of the portal sinus anatomy. Ultrasound Obstet Gynecol three-dimensional ultrasound in isolated vs. syndromal fetal
23:207–208. cleft lip/palate. Ultrasound Obstet Gynecol 29:265–270.
Peralta CFA, Falcon O, Wegrzyn P, Faro C, Nicolaides KH. Roelfsema NM, Grijseels EWM, Hop WCJ, Wladimiroff JW.
2005. Assessment of the gap between the fetal nasal bones at 2007c. Three-dimensional sonography of prenatal skull base
11 to 13 + 6 weeks of gestation by three-dimensional ultra- development. Ultrasound Obstet Gynecol 29:372–377.
sound. Ultrasound Obstet Gynecol 25:464–467. Roman AS, Monteagudo A, Timor-Tritsch I, Rebarber A. 2004.
Peralta CFA, Kazan-Tannus JF, Bunduki V, Santos EM, de First-trimester diagnosis of sacrococcygeal teratoma: the
Castrom C, Cerri GG, Zugaib M. 2006a. Evaluation of the role of three-dimensional ultrasound. Ultrasound Obstet
agreement between 3-dimensional ultrasonography and Gynecol 23:612–614.
magnetic resonance imaging for fetal lung volume measure- Rotten D, Levaillant JM. 2004a.Two- and three-dimensional
ment. J Ultrasound Med 25:461–467. sonographic assessment of the fetal face. A systematic
Peralta CFA, Cavoretto P, Csapo B, Falcon O, Nicolaides analysis of the normal face. Ultrasound Obstet Gynecol
KH. 2006b. Lung and heart volumes by three-dimensional 23:224–231.
ultrasound in normal fetuses at 12–32 weeks’ gestation. Rotten D, Levaillant JM. 2004b. Two- and three-dimensional
Ultrasound Obstet Gynecol 27:128–133. sonographic assessment of the fetal face. 2. Analysis of
Pilu G, Visentin A, Ambrosini G, D’Antona D, Andrisani A. 2005. cleft lip, alveolus and palate. Ultrasound Obstet Gynecol
Three-dimensional sonography of unilateral Tessier number 24:402–411.
7 cleft in a mid-trimester fetus. Ultrasound Obstet Gynecol Ruano R, Dumez Y, Dommergues M. 2003a. Three-dimensional
26:98–99. ultrasonographic appearance of the fetal akinesia deforma-
Pilu G, Segata M, Ghi T, Carletti A, Perolo A, Santini D, tion sequence. J Ultrasound Med 22:593–599.
Bonasoni P, Tani G, Rizzo N. 2006. Diagnosis of midline Ruano R, Benachi A, Aubry MC, Brunelle F, Dumez Y,
anomalies of the fetal brain with the three-dimensional Dommergues M. 2003b. Perinatal three-dimensional color
median view. Ultrasound Obstet Gynecol 27:522–529. power Doppler ultrasonography of vein of Galen aneurysms.
Pilu G, Segata M. 2007. A novel technique for visualiza- J Ultrasound Med 22:1357–1362.
tion of the normal and cleft fetal secondary palate: angled Ruano R, Joubin L, Sonigo P, Benachi A, Aubry, Thalabard JC,
insonation and three-dimensional ultrasound. Ultrasound Brunelle F, Dumezm Y, Dommergues M. 2004. Fetal lung
Obstet Gynecol 29:166–169. volume estimated by 3-dimensional ultrasonography and
Plasencia W, Dagklis T, Borenstein M, Csapo B, Nicolaides KH. magnetic resonance imaging in cases with isolated congeni-
2007. Assessment of the corpus callosum at 20–24 weeks’ tal diaphragmatic hernia. J Ultrasound Med 23:353–358.
gestation by three-dimensional ultrasound examination. Ruano R, Benachi A, Aubry M, Dumez Y, Dommergues M.
Ultrasound Obstet Gynecol 30:169–172. 2004a. Volume contrast imaging: a new approach to identify
Platt LD, DeVore GR, Pretorius DH. 2006. Improving cleft pal- fetal thoracic structures. J Ultrasound Med 23:403–408.
ate/cleft lip antenatal diagnosis by 3-dimensional sonography Ruano R, Molho M, Roume J, Ville Y. 2004b. Prenatal diagnosis
the “flipped face” view. J Ultrasound Med 25:1423–1430. of fetal skeletal dysplasias by combining two-dimensional
Pohls UG, Rempen A. 1998. Fetal lung volumetry by three- and three-dimensional ultrasound and intrauterine three-
dimensional ultrasound. Ultrasound Obstet Gynecol dimensional helical computer tomography. Ultrasound
11:6–12. Obstet Gynecol 24:134–140.
Ramón y Cajal CL, Ocampo Martínez R. 2003. Prenatal diagno- Ruano R, Martinovic J, Dommergues M, Aubry MC, Dumez Y,
sis of duodenal atresia with three-dimensional sonography. Benachi A. 2005a. Accuracy of fetal lung volume assessed
Ultrasound Obstet Gynecol 22:656–657. by three-dimensional sonography. Ultrasound Obstet
Ramón y Cajal CL, Martínez RO. 2005. Prenatal observation Gynecol 26:725–730.
of fetal defecation using four-dimensional ultrasonography. Ruano R, Benachi A, Aubry MC, Revillon Y, Emond S, Dumez
Ultrasound Obstet Gynecol 26:794–795. Y, Dommergues M. 2005b. Prenatal diagnosis of pulmonary
Rembouskos G, Cicero S, Longo D, Vandecruys H, Nicolaides sequestration using three-dimensional power Doppler ultra-
KH. 2004. Assessment of the fetal nasal bone at 11–14 weeks sound. Ultrasound Obstet Gynecol 25:128–133.
of gestation by three-dimensional ultrasound. Ultrasound Ruano R, Joubin L, Aubry MC, Thalabard JC, Dommergues, M,
Obstet Gynecol 23:232–236. Dumez Y, Benachi A. 2006. A nomogram of fetal lung vol-
Rizzo G, Capponi A, Muscatello A, Cavicchioni O, Vendola M, umes estimated by 3-dimensional ultrasonography using the
Arduini D. 2008. Examination of the fetal heart by four- rotational technique (virtual organ computer-aided analysis).
dimensional ultrasound with spatio temporal image cor- J Ultrasound Med 25:701–709.
relation during routine second-trimester examination: the Ruano R, Takashi E, Schultz R, Zugaib M. 2008. Prenatal diag-
“three-steps technique.” Fetal Diagn Ther 24:126–131. nosis of posterior mediastinal lymphangioma by two- and
Rochelson B, Vohra N, Krantz D, Macri VJ. 2006. Geometric three-dimensional ultrasonography. Ultrasound Obstet
morphometric analysis of shape outlines of the normal and Gynecol 31:697–700.
abnormal fetal skull using three-dimensional sonographic Ruano R, Pimenta EJ, Duarte S, Zugaib M. 2009. Four-
multiplanar display. Ultrasound Obstet Gynecol 27:167–172. dimensional ultrasonographic imaging of fetal lower urinary
Roelfsema NM, Hop WCJ, Wladimiroff JW. 2006. Three- tract obstruction and guidance of percutaneous cystoscopy.
dimensional sonographic determination of normal fetal Ultrasound Obstet Gynecol 33:250–252.
mandibular and maxillary size during the second half of Sabogal JC, Becker E, Bega G, Komwilaisak R, Berghella V,
pregnancy. Ultrasound Obstet Gynecol 28:950–957. Weiner S, Tolosa J. 2004. Reproducibility of fetal lung vol-
ume measurements with 3-dimensional ultrasonography. J
Ultrasound Med 23:347–352.
154 A Practical Guide to 3D Ultrasound
Sakhel K, Benson CB, Platt LD, Goldstein SR, Benacerraf BB. Tegnander E, Williams W, Johansen OJ, Blass HG, Eik-Nes SH.
2013. Begin with the basics: role of 3-dimensional sonog- 2006. Prenatal detection of heart defects in a non-selected
raphy as a first-line imaging technique in the cost-effective population of 30,149 fetuses—detection rates and outcome.
evaluation of gynecologic pelvic disease. J Ultrasound Med Ultrasound Obstet Gynecol 27:252–265.
32:381–388. Timor-Tritsch IE, Monteagudo A, Mayberry P. 2000. Three-
Sallout BI, D’Agostini DA, Pretorius DH. 2006. Prenatal diag- dimensional ultrasound evaluation of the fetal brain: the
nosis of spondylocostal dysostosis with 3-dimensional ultra- three horn view. Ultrasound Obstet Gynecol 16:302–306.
sonography. J Ultrasound Med 25:539–543. Tonni G, Lituania M. OmniView algorithm. 2012. A novel
Sammour RRN, Leibovitz Z, Degani S, Ohel G. 2008. Prenatal 3-dimensional sonographic technique in the study of the
diagnosis of small-bowel volvulus using 3-dimensional dop- fetal hard and soft palates. J Ultrasound Med 31:313–318.
pler sonography. J Ultrasound Med 27:1655–1661. Turan S, Turan OM, Ty-Torredes K, Harman CR, Baschat
Schild RL, Wallny T, Fimmers R, Hansmann M. 1999. Fetal AA. 2009. Standardization of the first-trimester fetal car-
lumbar spine volumetry by three-dimensional ultrasound. diac examination using spatiotemporal image correlation
Ultrasound Obstet Gynecol 13:335–339. with tomographic ultrasound and color Doppler imaging.
Schild RL, Plath H, Hofstaetter H, Hansmann M. 2000. Ultrasound Obstet Gynecol 33:652–656.
Diagnosis of a fetal mesoblastic nephroma by 3D-ultrasound. Turan S, Turan OM, Desai A, Harman CR, Baschat AA. 2014.
Ultrasound Obstet Gynecol 15:533–536. A prospective study of first trimester fetal cardiac examina-
Sepulveda W, Sandoval R, Carstens E, Gutierrez J, Vasquez P. tion using spatiotemporal image correlation, tomographic
2003. Hypohidrotic ectodermal dysplasia prenatal diagnosis ultrasound and color Doppler imaging for the diagnosis
by three-dimensional ultrasonography. J Ultrasound Med of complex congenital heart disease in high-risk patients.
22:731–735. Ultrasound Obstet Gynecol ePub Mar 1.
Sepulveda W, Sepulveda-Swatson E, Sanchez J. 2004. Uittenbogaard LB, Haak MC, Spreeuwenberg MD, van Vugt JM.
Diastrophic dysplasia: prenatal three-dimensional ultra- 2009. Fetal cardiac function assessed with four-dimensional
sound findings. Ultrasound Obstet Gynecol 23:312–314. ultrasound imaging using spatiotemporal image correlation.
Sepulveda W, Wojakowski AB, Elias D, Otaño L, Gutierrez J. Ultrasound Obstet Gynecol 33:272–281.
2005.Congenital dacryocystocele prenatal 2- and 3-dimen- United Healthcare. 2013. Clinical Policy. Obstetrical
sional sonographic findings. J Ultrasound Med 24:225–230. Sonography. https://www.oxhp.com/secure/policy/obstetri-
Sepulveda W. 2007. Prenatal 3-dimensional sonographic depic- cal_ultrasonography.pdf.
tion of the Wolf Hirschhorn phenotype. The “Greek Warrior Varvarigos E, Iaccarino M, Iaccarino S, Mucerino J. 2002.
Helmet” and “Tulip” signs. J Ultrasound Med 26:407–410. Transabdominal multiplanar scan vs. B-mode in examina-
Sepulveda W, Lutz I, Be C. 2007. Holoprosencephaly at 9 weeks tion of fetal physiologic brain sagittal scan. Ultrasound
6 days in a triploid fetus two- and 3-dimensional sonographic Obstet Gynecol 20:84.
findings. J Ultrasound Med 26:411–414. Verwoerd-Dikkeboom CM, Koning AHJ, Groenenberg IAL,
Shaw L, Al-Malt A, Carlan SJ, Plumley D, Greenbaum L, Kosko Smit BJ, Brezinka C, Van Der Spek PJ, Steegers EAP. 2008.
J. 2004. Congenital epulis three-dimensional ultrasono- Using virtual reality for evaluation of fetal ambiguous geni-
graphic findings and clinical implications. J Ultrasound Med talia. Ultrasound Obstet Gynecol 32:510–514.
23:1121–1124. Viñals F, Poblete P, Giuliano A. 2003. Spatio-temporal image
Sherer DM, Zigalo A, Abulafia O. 2006. Prenatal 3-dimensional correlation (STIC): a new tool for the prenatal screening
sonographic diagnosis of a massive fetal epignathus occlud- of congenital heart defects. Ultrasound Obstet Gynecol
ing the oral orifice and both nostrils at 35 weeks’ gestation. J 22:388–394.
Ultrasound Med 25:1503–1505. Viñals F, Muñoz M, Naveas R, Shalper J, Giuliano A. 2005.
Shih JC, Hsu WC, Chou HC, Peng SS, Chen LK, Chang YL, The fetal cerebellar vermis: anatomy and biometric assess-
Hsieh FJ. 2005. Prenatal three-dimensional ultrasound ment using volume contrast imaging in the C-plane (VCI-C).
and magnetic resonance imaging evaluation of a fetal oral Ultrasound Obstet Gynecol 26:622–627.
tumor in preparation for the ex-utero intrapartum treatment Viñals F, Ascenzo R, Poblete P, Comas C, Vargas G, Giuliano A.
(EXIT) procedure. Ultrasound Obstet Gynecol 25:76–79. 2006. Simple approach to prenatal diagnosis of transposition
Shipp TD, Mulliken JB, Bromley B, Benacerraf B. 2002. Three- of the great arteries. Ultrasound Obstet Gynecol 28:22–25.
dimensional prenatal diagnosis of frontonasal malformation Viñals F, Muñoz M, Naveas R, Giuliano A. 2007. Transfrontal
and unilateral cleft lip/palate. Ultrasound Obstet Gynecol three-dimensional visualization of midline cerebral struc-
20:290–293. tures. Ultrasound Obstet Gynecol 30:162–168.
Simioni C, Nardozza LM, Araujo Júnior E, Rolo LC, Zamith M, Viora E, Sciarrone A, Bastonero S, Errante G, Botta G,
Caetano AC, Moron AF. 2011. Heart stroke volume, cardiac Campogrande M. 2002. Three-dimensional ultrasound
output, and ejection fraction in 265 normal fetus in the sec- evaluation of short-rib polydactyly syndrome type II in the
ond half of gestation assessed by 4D ultrasound using spatio- second trimester: a case report. Ultrasound Obstet Gynecol
temporal image correlation. J Matern Fetal Neonatal Med 19:88–91.
24:1159–1167. Vohra N, Rochelson B, Smith-Levitin M. 2003. Three-
Soto E, Richani K, Gonçalves LF, Devers P, Espinoza J, Lee dimensional sonographic findings in congenital (Harlequin)
W, Treadwell MC, Romero R. 2006. Three-dimensional ichthyosis. J Ultrasound Med 22:737–739.
ultrasound in the prenatal diagnosis of cleidocranial dyspla- Volpe P, Buonadonna AL, Campobasso G, Di Carlo A, Stanziano
sia associated with B-cell immunodeficiency. Ultrasound A, Gentile M. 2004. Cat-eye syndrome in a fetus with
Obstet Gynecol 27:574–579. increased nuchal translucency: three-dimensional ultrasound
Tanaka Y, Miyazaki T, Kanenishi K, Tanaka H, Yanagihara T, and echocardiographic evaluation of the fetal phenotype.
Hata T. 2002. Antenatal three-dimensional sonographic Ultrasound Obstet Gynecol 24:485–487.
features of Treacher Collins syndrome. Ultrasound Obstet
Gynecol 19:414–415.
References 155
Volpe P, Contro E, DeMusso F, Ghi T, Farina A, Tempesta A, Volpe Youssef A, Bellussi F, Montaguti E, Maroni E, Salsi G, Maria
G, Rizzo N, Pilu G. 2012. Brainstem-vermis and brainstem- Morselli-Labate A, Paccapelo A, Rizzo N, Pilu G, Ghi T.
tentorium angles allow accurate categorization of fetal upward 2013. Agreement between two- and three-dimensional meth-
rotation of cerebellar vermis. Ultrasound Obstet Gynecol ods for the assessment of the fetal head-symphysis distance
39:632–635. in active labor. Ultrasound Obstet Gynecol 43:183–188.
Votino C, Cos T, Abu-Rustum R, Dahman Sidi S, Gallo V, Zalel Y, Yagel S, Achiron R, Kivilevich Z, Gindes L. 2009. Three-
Dobrescu O, Dessy H, Jani J. 2013. Spatio-temporal image dimensional ultrasonography of the fetal vermis at 18 to 26
correlation (STIC) modality at 11–14 weeks’ gestation. weeks’ gestation time of appearance of the primary fissure. J
Ultrasound Obstet Gynecol 42:669–678. Ultrasound Med 28:1–8.
Wong HS, Parker S, Tait J, Pringle KC. 2008. Antenatal diag- Zheng Y, Zhou XD, Zhu YL, Wang XL, Qian YQ, Lei XY, Chen
nosis of anophthalmia by three-dimensional ultrasound: a BL, Yu M, Xin XY. 2008. Three- and 4-dimensional ultraso-
novel application of the reverse face view. Ultrasound Obstet nography in the prenatal evaluation of fetal anomalies associ-
Gynecol 32:103–105. ated with trisomy 18. J Ultrasound Med 27:1041–1051.
Wong HS, Tait J, Pringle KC. 2009. Examination of the second- Zoppi MA, Ibba RM, Axiana C, Monni G. 2008. Prenatal sono-
ary palate on stored 3D ultrasound volumes of the fetal face. graphic features of isolated cleft soft palate with anterior axial
Ultrasound Obstet Gynecol 33:407–411. three-dimensional view reconstruction. Ultrasound Obstet
Yamamoto M, Essaoui M, Nasr B, Malek N, Takahashi Y, Moreira Gynecol 31:476–477.
de Sa R, Ville Y. 2007. Three-dimensional sonographic
assessment of fetal urine production before and after laser
surgery in twin-to-twin transfusion syndrome. Ultrasound
Obstet Gynecol 30:972–976.
Yeo L, Romero R. 2013. Fetal intelligent navigation echocar-
diography (FINE): a novel method for rapid, simple, and
automatic examination of the fetal heart. Ultrasound Obstet
Gynecol 42:268–284.
OBSTETRICS & GYNECOLOGY
Reem S. Abu-Rustum
K21746
ISBN: 978-1-4822-1433-8
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