Acute Lymphocytic Leukemia: Presented by Jacob Tabigo-On Mark Tapang
Acute Lymphocytic Leukemia: Presented by Jacob Tabigo-On Mark Tapang
Lymphocytic
Leukemia
Presented by
Jacob Tabigo-on
Mark Tapang
Introduction
Lymphoblasts stop the normal bone marrow production of red blood cells, platelets and mature
leucocytes resulting to thrombocytopenia, leukopenia, and anemia. Without treatment, the
client may die of infection or hemorrhage.
Physiology Review
Most blood cells are formed in the bone marrow, (the soft material in the center of most
bones) called stem cells.
Stem cells mature into different kinds of blood cells of which each kind has special functions:
a. White blood cells (also called WBCs or leukocytes), help the body fight infections and other
diseases.
b. Red blood cells (also called RBCs or erythrocytes) carry oxygen from the lungs to the bodys
tissues and take carbon dioxide from the tissues back to the lungs. The red blood cells give
blood its color.
c. Platelets (also called thrombocytes) help form blood clots that control bleeding
New or immature blood cells are called blasts. Some blasts stay in the marrow to mature while
some travel to other parts of the body to mature. When the blood cells grow old or get
damaged, they die, and new cells will form again. This picture shows how stem cells mature
into 2different types of white blood cells.
a. A myeloid stem cell matures into a myeloid blast, which further differentiate into
granulocytes, neutrophil, eosinophil and basophils
b. A lymphoid stem cell matures into a lymphoid blast which further differentiate into
lymphoid tissue such as B cells and T cells.
Leukemias are classified based on how quickly the disease develops and gets worse. It can be
either Chronic (which usually gets worse slowly) or Acute (which usually gets worse quickly)
a. Chronic leukemia
b. Acute leukemia
The types of leukemia also can be grouped based on the type of white blood cell that is
affected, namely lymphoid cells or myeloid cells:
A. Lymphocytic(or lymphoblastic)
Leukemias involve immature lymphocytes and their precursor cells in the bone marrow. It also
penetrates the spleen, lymph nodes, CNS and other tissues.
This involves the myeloid stem cells in the bone marrow, intervening with the maturation of all
types of blood cells, including granulocytes, RBCs, and thrombocytes. This affects mostly on
adult people.
Epidemiology
ALL is the most common type of childhood cancer. It most often occurs in children ages 3 to 5
and affects slightly more boys than girls.
About 3,000 people younger than age 20 are found to have ALL each year in the United States.
Siblings of children with leukemia have a slightly higher risk of developing ALL, but the rate is
still quite low: no more than 1 in 500.\
The incidence of ALL appears to be highest in Hispanic children (43 cases per 1 million).
The incidence is substantially higher in white children than in black children, with a nearly
threefold higher incidence of ALL from age 2 to 3 years in white children than in black children
Predisposing Factors
The exact cause of leukemia is not clear. However, few have been associated with an increased
risk of developing the disease:
Radiation: People exposed to very high levels of radiation are much more likely than others to
get acute myeloid leukemia, chronic myeloid leukemia, or acute lymphocytic leukemia. (e.g.
Atomic bomb explosions, Radiation therapy, Diagnostic X-rays)
Chemotherapy: Cancer patients treated with certain types of cancer-fighting drugs sometimes
later get acute myeloid leukemia or acute lymphocytic leukemia e.g., alkylating agents or
topoisomerase inhibitors is linked with a small chance of later developing acute leukemia.
Down Syndrome and certain other inherited disease increase the risk of acute leukemia
Patients Profile
Name: I.L.
Birthdate: 02/03/2002
Gender: Male
Social History
Patient lives with his parents and older sibling; daily activities include watching tv, attending
school and playing outside.
Family History
Maternal Benign breast cyst, breast cancer, goiter
2. Nutritional and
Metabolism
3. Elimination Pattern
4. Activity-Exercise Pattern
7. Self-Perception- Self
Concept
8. Role-Relationship Pattern
9. Sexuality-Reproductive
Pattern
Laboratory Results
Test Results Normal Range
Specimen CFS
WBC 1 X10^g/L
Lymphocyte 100%
Neutrophil
RBC 1,800 X10^g/L
Prothrombin Time 14.1 sec 10-15
Control 12.0 sec
INR 1.18
% Activity 78.1
Partial thromboplastin time 31.3 sec 29-34
Control 30.0
Bleeding Time 200 min 1-3
Clinical Manifestations
Leukemia like other blood cells, travel through the body where it influences the health and
function of all organs and systems.
Symptoms may vary from one person to another, depending on the number of leukemic cells
and where these cells collect in the body. But generally, manifestation of leukemia results from
anemia, infection and bleeding.
These include pallor, fatigue, tachycardia, malaise, lethargy, and dyspnea on exertion.
Lost of appetite
Joint/Bone pain
Weakness
Hepatomegaly
Systemic Infections
Bleeding
Anemia
Headache
Vomiting
Lymphadenopathy
Seizures
Clinical Investigations
o Physical Exam - Checks for swollen lymph nodes, spleen, or liver.
o Blood Tests Complete blood count to check the number of white blood cells, red
blood cells, and platelets. Leukemia causes a very high level of white blood cells. It may
also cause low levels of platelets and hemoglobin, which is found inside red blood cells.
o Biopsy - Removal of tissue of the bone marrow in the hipbone or other large bone to
look for cancer cells. It is the only way to know whether leukemia cells are in the bone
marrow. There are two ways how to obtain sample of the bone marrow, some physician
do both at the same time:
1. Bone Marrow Aspiration - The doctor uses a thick, hollow needle to remove samples
of bone marrow.
2. Bone Marrow Biopsy - The doctor uses a very thick, hollow needle to remove a small
piece of bone and bone marrow.
o Chemotherapy - This is the treatment choice of most types of leukemia, with a goal
of eradicating leukemic cells and producing remission. Children with this disease are
likely to be cured and a number of adult patients have high remissions. Generally,
chemotherapy is divided into 2 phases: induction phase therapy and post-remission
therapy
a. Induction Phase.
During this phase drugs doses are high to eradicate leukemic cells from the bone
marrow. A combination of drugs is used such as daunorubin (cerubidine, an antitumor
antibiotic) with vincristine (oncovin, a plant alkaloid) with prednisone with asparaginase
(elspar).
These high doses of drug often damage the stem cells and interfere with the production
of normal blood cells but circulating mature blood cells are not affected because they
are no longer dividing.
b. Post-remission Therapy.
o Radiation Therapy
(also called radiotherapy) uses high-energy rays to kill leukemia cells. Radiotherapy
damages cellular DNA.
Though the leukemic cells continue to function, it cannot divide and multiply e.g., cells
in bone marrow and cancer cells divides rapidly and respond quickly to radiation
therapy.
Radiotherapy is also aimed at the spleen, the brain, or other parts of the body where
leukemia cells have collected.
o Biologic Therapy
Interferon and interleukin (cytokines) may be used to treat leukemias. They modify the
bodys response to cancer cells, moderate immune function and inhibit abnormal cell
proliferation and growth.
1. Allogenic BMT.
Uses the bone marrow of a healthy donor (usually from a sibling/unrelated closed
matched antigen. The donors bone marrow is aspirated and is infused through a central
venous line into the recipient.
Uses the client own bone marrow to restore the bone marrow function after
chemotherapy or radiation. During the period of disease remission, about 1L of bone
marrow is aspirated from the patient. It is then stored and frozen for use after
treatment of chemotherapy or radiation, with the aim of destroying the immune system
and malignant cells and to prepare space in the bone marrow for new cells.
The filtered bone marrow is thawed and infused intravenously through central line and
slowly become part of the clients bone marrow, neutrophil count increases, and normal
haematopoiesis takes place.
The recipient and the donor tissue must be closely matched prior to harvesting and
necessary procedure and treatment are conducted prior to harvesting to prevent the
risk of infection and other complications
Medications
Name Mechanism of Indication Contraindication Side Nursing
Action
effects Responsibility
O> Weak in Risk for After 6 hours of -Observed -To be able to After 6 hours of
appearance, infection r/t nursing localized signs know the nursing
undergone post intervention, of infection existence of intervention,
circumcision operational the client will infection the client
with open wound remain free remained free
wound, 100/60, from any signs -Encouraged from any signs
of infection. mother to limit -To limit of infection
36.5 C, 98,17
visitors spread of
infection in
the room
-Taught client
on proper hand
washing and
-To prevent
perineal care.
spread of
-Instructed bacteria
client on how
to perform
correct way of -To promote
dressing the comfort
wound