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Acute lymphocytic leukemia (ALL)

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Illustrations

Bone marrow aspiration
Bone marrow aspiration
Acute lymphocytic leukemia - photomicrograph
Acute lymphocytic leukemia - photomicrograph
Auer rods
Auer rods
Bone marrow from hip
Bone marrow from hip
Immune system structures
Immune system structures

Alternative Names    Return to top

ALL; Acute childhood leukemia; Cancer - acute childhood leukemia (ALL); Leukemia - acute childhood (ALL)

Definition    Return to top

Acute lymphocytic leukemia (ALL) is a fast-growing cancer in which the body produces a large number of immature white blood cells (lymphocytes). These cells can be found in the blood, bone marrow, lymph nodes, spleen, and other organs.

Causes    Return to top

ALL makes up 80% of childhood acute leukemias. Most cases occur in children ages 3 - 7. The disease may also occur in adults.

In acute leukemia, cancerous cells multiply quickly and replace normal cells. Cancerous cells take over normal parts of bone marrow, causing bone marrow failure. A person with ALL is more likely to bleed and have infections because there are fewer normal blood cells.

Most cases of ALL have no obvious cause. However, chromosome problems, radiation, toxins such as benzene, and some chemotherapy drugs may play a role in the development of leukemia.

Persons with Down syndrome or who have a brother or sister with leukemia have an increased risk for ALL.

Symptoms    Return to top

Exams and Tests    Return to top

A physical exam may reveal the following:

Blood tests may show the following:

A bone marrow aspiration may be show abnormal levels of certain cells.

ALL may also change the results of the following tests:

If you are diagnosed with ALL, genetic tests will be done to determine the specific type of ALL. Doctors can look for chromosome changes in the cells of some leukemias. Leukemias with certain types of chromosome changes have a poor outlook, while those with other types of genes can have a very good outlook.

Treatment    Return to top

The goal of treatment is to get the blood counts and the bone marrow to normal. If this occurs, the cancer is considered to be in remission.

If you have acute lymphocytic leukemia, you'll need chemotherapy. For the first round of chemotherapy, you may need to go to the hospital for 3 - 6 weeks, but may later get chemotherapy on an outpatient basis. If you have a low white blood cell count, you may need to be placed in a room by yourself so you do not catch an infection.

Additional treatments depend on other symptoms. They may include:

If you go into remission, you may receive additional chemotherapy or radiation therapy to kill any cancer cells that are in the spinal fluid. You may also receive chemotherapy from time to time to prevent relapse.

If your leukemia returns or does not respond to other treatments, your doctor may recommend a bone marrow transplant after high-dose chemotherapy.

High-risk patients may need bone marrow or stem cell transplants.

Support Groups    Return to top

Patients can ease the stress of their illness by joining a support group where members share common experiences and problems.

See also: Cancer - support group

Outlook (Prognosis)    Return to top

Children usually have a better outcome than adults. The majority of adults go into complete remission. Without treatment, a person with ALL can expect to live for about 3 months.

Possible Complications    Return to top

When to Contact a Medical Professional    Return to top

Call your health care provider if you develop ALL-like symptoms, or if you have ALL and you have a persistent fever or other signs of infection.

Prevention    Return to top

Because the cause is usually unknown, it is not possible to prevent most cases. You may reduce your risk of ALL by avoiding exposure to toxins, radiation, and chemicals.

References    Return to top

American Cancer Society. Cancer Facts and Figures 2007. Atlanta, GA: American Cancer Society; 2007.

National Cancer Institute. Adult acute lymphoblastic leukemia treatment (PDQ). 2008. Accessed June 10, 2008.

Update Date: 6/10/2008

Updated by: James R. Mason, MD, Oncologist, Director, Blood and Marrow Transplantation Program and Stem Cell Processing Lab, Scripps Clinic, Torrey Pines, California. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

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