Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases, Updated Edition - Periocular Infections PDF
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases, Updated Edition - Periocular Infections PDF
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases, Updated Edition - Periocular Infections PDF
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1433
Periosteum
Tarsal plate
Meibomian gland
Gland of Zeis
Dacryoadenitis
Dacryoadenitis is an inflammation of the lacrimal gland. Infections are
rare and may be acute or chronic. Patients with acute dacryoadenitis
present with a tender area of erythema and swelling in the lateral part
of the upper lid. It may lead to preseptal or orbital cellulitis or may
suppurate into an abscess.18,19 S. aureus is the most common pathogen,
although streptococci may also be a cause.20 A recent series of 11 cases
of acute bacterial dacryoadenitis with positive cultures from lid aspi-
rate, biopsy, or purulent drainage reported S. aureus in over half
FIGURE 118-3 Photograph of eyelids with marginal blepharitis. (6 cases), followed by Streptococcus pneumoniae (2), mixed skin flora
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1434
Lacrimal gland Puncta of the canaliculus. Occasionally, surgical exploration is required. Anti-
biotics given topically as eyedrops (ciprofloxacin plus cefazolin) several
times daily, with or without irrigation of the canaliculi with antibiotics,
was effective in all patients in one series from India.48
Part II Major Clinical Syndromes
Dacryocystitis
Lacrimal sac Dacryocystitis, or inflammation of the lacrimal sac, is the most
common infection of the lacrimal system. It arises because of obstruc-
Canaliculum tion of the lacrimal duct, pooling of tears in the lacrimal sac, and
Lacrimal duct subsequent infection. Obstruction may be congenital or may result
(lies in bone)
from trauma, tumors, infection, or inflammation of the duct. Acute
dacryocystitis symptoms include pain, swelling, and erythema near the
nasal corner of the eye. There is usually epiphora (excessive tearing)
and a purulent discharge. Infants often have lacrimal duct obstruction
with epiphora, but acute dacryocystitis complicates the obstruction in
only 3%.49 The most common causes of acute dacryocystitis are S.
aureus and streptococci. Gram-negative bacilli accounted for 25% of
Inferior nasal isolates in one study, with Escherichia coli as the most frequent gram-
turbinate negative organism isolated.50 Treatment requires antibiotic therapy
FIGURE 118-5 The lacrimal system. (Modified from Barza M, Baum (e.g., ampicillin-sulbactam) and usually incision and drainage of a
J. Ocular infections. Med Clin North Am. 1983;67:131-152.) lacrimal sac abscess. In one study, incision and drainage was an out-
patient procedure requiring only local anesthesia in approximately
80% of cases.51 A repeat drainage procedure was required within 1
(2), and Haemophilus influenzae (1).21 There are case reports of acute month in 8%. Chronic or recurrent dacryocystitis usually requires a
suppurative dacryoadenitis due to Pseudomonas, brucellosis, and surgical procedure, dacryocystorhinostomy (DCR). One study found
cysticercosis.22-24 Epstein-Barr virus may cause acute nonsuppurative that cultures taken at the time of DCR surgery were positive in nearly
dacryoadenitis in mononucleosis, which may be unilateral or bilat- half of the 114 patients studied, although only one fifth of the patients
eral.25,26 It may result in keratoconjunctivitis sicca.27 Acute herpes had a history of dacryocystitis.52 Staphylococcus epidermidis and S.
zoster dacryocystitis was described in a patient who, 2 days later, devel- aureus were the only organisms isolated in 45% and 24% of culture-
oped iridocyclitis and shingles in the distribution of the first division positive cases. Whether these reflect nasal flora contamination is
of the trigeminal nerve.28 A study found that dacryoadenitis was unknown. Gram-negative bacilli composed a larger percentage of iso-
present in one third of patients with Acanthamoeba keratitis, although lates in patients with a history of dacryocystitis, a finding also noted
direct infection of the lacrimal gland was not found.29 Chronic infec- by others.53 Gram-negative bacilli were present in 26% of cultures in a
tious dacryoadenitis is rare, but most reports describe Mycobacterium recent study, with H. influenzae predominating.54 Anaerobes were
tuberculosis as the cause.30-32 Most cases of chronic dacryoadenitis are found in 19%. Fungi have been reported as a cause of two cases of
inflammatory rather than infectious, however. Sjögren’s disease and dacryocystitis, including one with mucormycosis involving the lacri-
sarcoidosis are the most common associated diseases, although cases mal sac.55 Rhinosporidium seeberi, an aquatic protistan parasite seen
of Crohn’s disease and Wegener’s disease presenting as chronic dacryo- especially in tropical climates such as southern India, may cause
adenitis have been described.33,34 Granulomatous inflammation of chronic dacryocystitis. A recent report from India described 50 patients
bilateral lacrimal glands was seen in one patient receiving interferon-α seen with ocular rhinosporidiosis over a 2.5-year period; half had
and ribavirin for hepatitis C; evaluation for sarcoidosis was negative.35 conjunctival involvement, and 26% had lacrimal sac involvement.56
Tumors cause approximately 25% of cases of chronic lacrimal gland Bloody discharge from the puncta was a feature of lacrimal sac infec-
enlargement.20 tion, and at surgery, a pink, vascularized growth was found in the
lacrimal sac.
Canaliculitis Patients with an episode of acute dacryocystitis who do not ulti-
Canaliculitis may occur spontaneously or develop after placement of mately undergo a DCR procedure may have further episodes of acute
silicone in the canaliculi (e.g., punctal plugs to treat dry eyes) or in the dacryocystitis. One study found that 4 of 16 patients with a lacrimal
nasolacrimal system (tubes for tear drainage). Infections have also abscess who did not eventually have a definitive procedure (DCR or
been associated with the more recent types of canalicular plugs made dacryocystectomy) developed a recurrent lacrimal sac abscess.51
from a temperature-sensitive acrylic polymer.36 Canaliculitis results in
chronic symptoms of tearing and irritation in the medial portion of PRESEPTAL CELLULITIS AND
the affected eyelid. Examination reveals a swollen, “pouting” punctum ORBITAL INFECTIONS
and erythema of the adjacent nasal conjunctiva. There may be a uni- Anatomy
lateral conjunctivitis. The lower canaliculus is affected more often than The orbital septum is a thin, fibrous membrane that serves as a barrier
the upper.20 A yellow-green exudate and yellowish concretions may be between the superficial lids and the orbit. The septum arises from the
expressed from the involved punctum in many cases of canaliculitis. orbital periosteum at the orbital rim and extends to the tarsal plates of
The concretions, called sulfur granules, are formed by Actinomyces the eyelids (see Fig. 118-1). Infections anterior to the septum are pre-
israelii, the organism in the majority of cases.37 A recent review of the septal, and infections posterior to the septum are orbital. Preseptal
literature found that of 188 reported cases, Actinomyces (30% of cases), cellulitis involves only the lids and not the orbit, whereas orbital cel
streptococci (12%), and staphylococci (10%) were the most common lulitis involves the soft tissues (fat, muscle) contained within the bony
etiologies, while cultures were negative in 22%.38 In a series from India orbit (Fig. 118-6). The bony orbit is shaped like a cone placed horizon-
of 74 patients with primary canaliculitis, staphylococci were cultured tally, apex tilted medially. It is surrounded by the paranasal sinuses for
in 39% of cases.39 Mycobacterium chelonae has been the etiology in much of its circumference: the frontal sinus superiorly, the maxillary
several cases, usually associated with punctal plugs.40,41 Rare causes sinus inferiorly, and the ethmoid medially. The medial orbital wall, the
include Propionibacterium propionicum,42 Eikenella corrodens, either paper-thin lamina papyracea, is also the lateral wall of the ethmoid
alone43 or with Streptococcus anginosus (milleri) group,44 Arcanobacte sinus. It contains multiple foramina for nerves and blood vessels and
rium haemolyticum,45 Enterobacter cloacae,46 and Nocardia asteroides.47 natural defects called Zuckerkandl’s dehiscences. For these anatomic
Nocardia was found in canalicular cultures of 5 of 12 canaliculitis reasons, ethmoid sinusitis is the most common cause of sinus-related
patients in a series from Chennai, India.48 Treatment requires removal orbital infection. Periosteum (periorbita) lines the orbit, and infection
of canalicular material and concretions, usually accomplished by from the ethmoid sinus may cross the lamina papyracea and collect
applying pressure near the nasal corner of the eye or by office curettage beneath the periorbita as a subperiosteal abscess. Infection may break
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1435
Preseptal cellulitis Orbital cellulitis The etiology of sinus-related preseptal and orbital cellulitis is usually
unknown because blood cultures are often negative. Sinus cultures in
these cases reveal typical acute sinusitis pathogens, such as S. pneu
moniae and H. influenzae. Some studies show S. aureus as a major
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1436
erythematosus or hematologic disorders.85 Patients with lupus who syndrome in immunocompromised or normal hosts and may have a
develop this may just have started corticosteroid therapy. Pneumococ- subacute presentation.91,92 Pseudallescheria boydii has been described
cal orbital cellulitis has also been described in a previously healthy as an etiology in rare cases of invasive fungal infection involving the
adult without bacteremia.86 Pseudomonas preseptal or orbital cellulitis orbital apex.93 Rare cases of orbital apex syndrome are due to
Part II Major Clinical Syndromes
may occur in neutropenic cancer patients secondary to Pseudomonas bacteria.94-96 Visual loss is usually irreversible.
bacteremia.87,88 If the infection is localized immediately anterior to the orbital apex,
a “superior orbital fissure syndrome” may occur. This syndrome has the
Clinical Manifestations same cranial neuropathies as orbital apex syndrome except there is no
Preseptal and Orbital Cellulitis involvement of the optic nerve. If the infection is posterior to the orbital
Preseptal cellulitis must be distinguished from orbital cellulitis, a much apex, a “cavernous sinus syndrome” may occur. This has the same
more dangerous infection. The term periorbital cellulitis, sometimes cranial neuropathies as orbital apex syndrome except with the added
used for preseptal cellulitis, should be avoided because it does not involvement of the second division of cranial nerve V and sometimes
make this distinction clear. In preseptal and orbital cellulitis, the lids the oculosympathetic fibers. In addition, because the cavernous sinus
are red and swollen. The lids may be swollen shut, but it is essential to is a venous plexus that extends to the opposite side, bilateral cranial
examine the eye to evaluate visual acuity and extraocular movement. neuropathies are typical. The superior orbital fissure, orbital apex, and
In preseptal cellulitis, vision is normal, there is no afferent pupillary cavernous sinus are contiguous and the etiologies are similar.89 Infec-
defect, extraocular movements are full and painless, and there is no tions rarely respect the precise anatomic locations these syndromes
proptosis. In contrast, patients with orbital cellulitis have some degree imply, and infections may be in the cavernous sinus, for example,
of ophthalmoplegia or proptosis, or both. There is often deep eye pain without having all the features of the cavernous sinus syndrome. Infec-
and pain with eye movement. Proptosis may not be grossly apparent tious etiologies for all of these syndromes include fungi, bacteria such
and should be measured (e.g., with Hertel’s exophthalmometer); a dif- as S. aureus, streptococci including S. anginosus (milleri), gram-negative
ference of 2 mm or more is significant. Vision may be decreased, and bacilli, syphilis, and herpes zoster. Herpes zoster ophthalmicus (HZO)
an early warning sign may be an afferent pupillary defect. Fever and may rarely be complicated by complete unilateral ophthalmoplegia or
leukocytosis are usually present in children with preseptal or orbital orbital apex syndrome. In a review of 20 cases, HZO preceded ophthal-
cellulitis, but they may be absent in adults. Fever was present in 70% moplegia in 75% and occurred concurrently in 20%.97
of pediatric cases but only 30% of adult cases in one series.62
Cavernous Sinus Thrombophlebitis
Orbital and Subperiosteal Abscesses Septic cavernous sinus thrombophlebitis is rare and should be sus-
Patients with an orbital or subperiosteal abscess usually present with pected in any patient with orbital cellulitis who develops contralateral
marked lid swelling and erythema, eye pain, proptosis, marked oph- signs of orbital inflammation (lid swelling, proptosis, ophthalmople-
thalmoplegia, and often vision loss. Most have fever. Because the gia) (see also Chapter 93). Spread to the opposite eye occurs through
abscess is medial or superomedial in nearly all cases, the eye is typically the cavernous sinus and usually occurs within 24 to 48 hours of the
fixed looking “down and out” (Fig. 118-7). initial unilateral orbital findings.98 Patients may also present with bilat-
eral findings, including lid edema, chemosis, proptosis, ptosis, and
Orbital Apex, Superior Orbital Fissure, and ophthalmoplegia, or they may present with signs of bilateral neuropa-
Cavernous Sinus Syndromes thies of some or all of cranial nerves III, IV, and VI but without the lid
Orbital apex syndrome is characterized by marked ophthalmoplegia edema and erythema that typifies orbital cellulitis. The latter is espe-
and vision loss. The cranial nerves of the orbital apex are involved, cially true in cases of cavernous sinus thrombophlebitis that arise from
which include the optic nerve and cranial nerves III, IV, VI, and the skin infections of the mid third of the face, or in dental infections,
first division of V. There is often an afferent pupillary defect due to rather than primary orbital infections. In cavernous sinus thrombo-
involvement of the optic nerve and hypoesthesia of the forehead phlebitis, there may be decreased sensation over the forehead and
due to involvement of the first division of cranial nerve V. Etiologies sometimes cheek due to involvement of the first or second division of
include vascular (e.g., carotid cavernous fistula); inflammatory (e.g., cranial nerve V. Trigeminal nerve involvement may be seen in a quarter
giant cell arteritis, Wegener’s disease); neoplastic (e.g., lymphoma, of patients with cavernous sinus thrombophlebitis but is not a feature
head and neck cancers, neural tumors); and infectious.89 In infectious of usual bacterial orbital cellulitis.99 Early cases may present with uni-
orbital apex syndrome, unlike orbital cellulitis, marked vision loss lateral findings of orbital cellulitis and cavernous sinus syndrome but
and ophthalmoplegia may occur with minimal or no lid swelling or with persistent headache and lethargy. This was illustrated in a recent
erythema. Overt signs of orbital inflammation may worsen subse- case report of a child with cavernous sinus thrombophlebitis, sphenoid
quently. This syndrome is usually caused by infection in the adjacent sinusitis, and S. anginosus (milleri) bacteremia in whom the clues to
posterior ethmoid or sphenoid sinuses, and most cases are due to more serious infection were unrelenting headache, fever, and leth-
invasive mold infections. Orbital apex syndrome is a well-known pre- argy.100 Visual loss may occur from venous congestion and ischemia.
sentation of mucormycosis.90 Aspergillus may cause an orbital apex Patients are usually febrile and may be lethargic or obtunded. There is
often sphenoid and posterior ethmoid sinusitis. S. aureus is the major
pathogen, and cases of methicillin-resistant S. aureus have also been
described.101 Other pathogens include streptococci, especially S. angi
nosus (milleri) group, anaerobes, and gram-negative bacilli.102-104 Two
cases with a subacute presentation involved Actinomyces in one
and Aggregatibacter (Actinobacillus) actinomycetemcomitans in the
other.105,106 In both cases, patients initially were misdiagnosed as having
Tolosa-Hunt syndrome, an idiopathic, steroid-responsive inflamma-
tory process involving the cavernous sinus.
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1437
vision, or a combination of these) because it is essential to identify an of 8 patients with cavernous sinus thrombophlebitis and 30 control
abscess that may require urgent drainage. Repeat scans should also be patients, 2 independent radiologists blinded to the cases reviewed the
obtained in any patient with presumed uncomplicated orbital cellulitis CT images.112 They correctly diagnosed 7 of the 8 patients with cavern-
who fails to improve, or worsens, on intravenous antibiotics alone. A ous sinus thrombosis on initial CT images and correctly diagnosed the
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1438
intravenous antibiotics only if vision is normal and close monitoring Broad-spectrum combination antibiotic therapy (e.g., vancomycin,
is possible.107 Surgical drainage does not always require an external metronidazole, ceftriaxone) should also be used as initial therapy for
incision. A nasal endoscopic approach has proved successful in drain- acute bacterial cavernous sinus thrombosis until culture results are
ing medial subperiosteal abscesses in some patients.107,118 available. Because this infection carries a high risk of intracranial com-
Part II Major Clinical Syndromes
All patients with orbital abscesses should have immediate surgical plications (e.g., brain abscess, subdural empyema), any regimen should
drainage, in addition to initial broad-spectrum empirical therapy. include antibiotics that cross the blood-brain barrier. In septic cavern-
Combination therapy with vancomycin, metronidazole, and ceftriax- ous sinus thrombosis, surgical drainage of the primary focus of infec-
one will provide coverage for most pathogens; it is usually important tion (e.g., sinusitis or dental abscess) should be performed and patients
to initially include an antibiotic active against MRSA given the increas- should be monitored closely for any intracranial extension that may
ing incidence of this organism. Antibiotics may be simplified (e.g., to require surgical drainage.118a The use of anticoagulation has been con-
ampicillin-sulbactam) following drainage if cultures reveal sensitive troversial, but some studies suggested it was beneficial when started
organisms. early in patients who had no evidence of hemorrhage.119,120
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1438.e1
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