Acute lymphocytic leukemia

Causes and Risks:
Acute lymphocytic leukemia (A.L.L.) is responsible for 80% of the acute leukemias of childhood, with the peak incidence occurring between ages 3 and 7. A.L.L. also occurs in adults, where it comprises 20% of all adult leukemias. In acute leukemia, the malignant cell loses its ability to mature and specialize (differentiate) its function. These cells multiply rapidly and replace the normal cells. Bone marrow failure occurs as malignant cells replace normal bone marrow elements. The person becomes susceptible to bleeding and infection because the normal blood cells are reduced in number.

Most cases seem to have no apparent cause. However, radiation, some toxins such as benzene, and some chemotherapy agents are thought to contribute to the induction of leukemia . Abnormalities in chromosomes may also play a role in the development of acute leukemia. Risk factors for acute leukemia include Down syndrome , a sibling with leukemia, and exposure to radiation, chemicals, and drugs. The incidence is 6 out of 100,000 people.

Prevention:
Because the cause of most cases is unknown, prevention of most cases is unknown. Minimizing exposure to toxins , radiation, chemicals, and so on may reduce risk.

Symptoms:



Signs and Tests:
Physical examination shows enlarged liver and spleen, bruising (ecchymosis) and evidence of bleeding ( petechiae , purpura , and so on).

This disease may also alter the results of the following tests:



Treatment:
The goal of treatment is remission of the cancer . A remission is achieved when the peripheral blood counts and the bone marrow are normal.

Acute lymphocytic leukemia is treated with a combination of anti-cancer drugs ( chemotherapy ). A hospitalization of three to six weeks may be necessary for initial (induction) chemotherapy, however, subsequent chemotherapy sessions may be administered on an outpatient basis. Additionally, isolation procedures may be necessary if the lymphocyte count is very low to prevent exposure to infectious agents.

Chemotherapy typically consists of a combination of 3 to 8 medications which may include: prednisone, vincristine, methotrexate, 6-mercaptopurine, and cyclophosphamide. It may also be necessary to administer blood products (e.g., packed red blood cells, platelets ) to correct the anemia and low platelet count . Antibiotic therapy may be required to treat any secondary infections that develop.

After remission is achieved, chemotherapy and/or radiation therapy is administered in the spinal column to treat any leukemic cells that may have invaded the spinal fluid.

Subsequent therapy is directed at preventing relapse. A bone marrow transplant after high-dose chemotherapy is a treatment option for cases that relapse or do not respond to other treatments. The usual cost of a bone marrow transplant ranges from $150,000 to $200,000.

Support group :
The stress of illness can often be helped by joining a support group where members share common experiences and problems. See cancer - support group and leukemia - support group .

Prognosis:
The probable outcome for children is better than for adults, with approximately 95% achieving complete remission and a cure rate of 50% to 60%. Eighty percent of adults achieve complete remission, with 30% to 50% being cured. Without treatment, the life expectancy is about 3 months.

Complications:



Call Your Healthcare Provider:
Call for an appointment with your health care provider if symptoms suggestive of A.L.L. develop.

Call your health care provider if persistent fever or other signs of infection occur in a person with A.L.L.


This picture shows the darkly-stained lymph cells (lymphoblasts) seen in acute lymphocytic leukemia (ALL), the most common type of childhood leukemia.