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From Nemours' KidsHealth
- Non-Hodgkin Lymphoma
- Acute Myeloid Leukemia (AML)
- Stem Cell Transplants
- Acute Lymphoblastic Leukemia (ALL)
- Hodgkin Lymphoma
- Juvenile Myelomonocytic Leukemia (JMML)
- Wilms Tumor
- Aspiration and Biopsy: Bone Marrow
- Chronic Myelogenous Leukemia (CML)
- Cord-Blood Banking
- Alpha Thalassemia
- Childhood Cancer
- Sickle Cell Disease
- Severe Combined Immunodeficiency
- Iron-Deficiency Anemia
- Beta Thalassemia
Trusted External Resources
- National Marrow Donor Program
- Blood & Marrow Transplant Information Network
- National Bone Marrow Transplant Link
- The Bone Marrow Foundation
- Center for International Blood & Marrow Transplant Research (CIBMTR)
- American Cancer Society
- The National Children's Cancer Society- Beyond the Cure
- Survivorship Guidelines
- CHILD Cancer Fund
- Children’s Oncology Group
- Dreams Come True
- Leukemia & Lymphoma Society
- Make-A-Wish Foundation
- National Cancer Institute
- National Institutes of Health
Juvenile Myelomonocytic Leukemia (JMML)
Leukemia is a type of cancer that affects the body's white blood cells (WBCs).
Normally, WBCs help fight infection and protect the body against disease. But in leukemia, WBCs turn cancerous and multiply when they shouldn't, resulting in too many abnormal WBCs, which then interfere with the body's ability to function normally.
Juvenile myelomonocytic leukemia (JMML) is a rare childhood cancer that usually occurs in children younger than 2 years old. In JMML, too many myelocytes and monocytes (two types of WBCs) are produced from immature blood stem cells called blasts. These myelocytes, monocytes, and blasts overwhelm the normal cells in the bone marrow and other organs, causing the symptoms of JMML.
The cause of JMML is unknown, but doctors do know that certain medical conditions — such as neurofibromatosis type 1 and Noonan syndrome — can make a child more likely to develop it.
Signs and Symptoms
JMML tends to progress slowly, so at first a child may have few if any symptoms. In fact, symptoms can take months or even years to develop.
The symptoms of all types of leukemia are generally the same and include:
- fatigue and weakness
- swollen lymph nodes
- recurrent infections (such as bronchitis or tonsillitis)
- easy bruising
- bone and joint pain
- abdominal pain (caused by abnormal blood cells accumulating in organs like the kidneys, liver, and spleen)
A doctor who suspects a child has leukemia may order tests that include:
- Blood tests. Tests such as a complete blood count, liver and kidney function panels, and blood chemistries can give important information about the number of normal blood cells in the body and how well the organs are functioning. The blood cells will also be examined under a microscope to check for abnormal shapes or sizes.
- Bone marrow aspiration. In this procedure, the doctor inserts a needle into a large bone, usually the hip, and removes a small amount of bone marrow to examine it for abnormal cells.
- Imaging studies. These may include an X-ray, CT scan, MRI, or ultrasound to check for an enlarged spleen or liver, and also to rule out any other possible causes of a child's symptoms.
- Lumbar puncture. Also called a spinal tap, this procedure uses a hollow needle to remove a small amount of cerebrospinal fluid (the fluid surrounding the brain and spinal cord) for examination in a lab.
- Flow cytometry tests. By analyzing the properties of the cancer cells, doctors can determine the type of leukemia a child has. This is important because treatment varies among different types of leukemia.
- Chromosomal tests. By analyzing DNA from the blood or bone marrow, doctors can determine the type of leukemia a child has. This is important because treatments may vary according to the type of leukemia.
- Tissue typing or HLA (human leukocyte antigen) typing. If a child needs a stem cell transplant (also called a bone marrow transplant), this test helps doctors find a suitable stem cell donor. It works by comparing the proteins on the surface of a child's blood cells with the proteins on a potential donor's cells. The more "HLA markers" a child and donor share, the greater the chance that a transplant will be successful.
Chemotherapy (the use of drugs to kill cancer cells) may be used to temporarily control JMML. However, effective treatment of JMML usually requires a stem cell (bone marrow) transplant.
This procedure involves destroying cancer cells and normal bone marrow and immune system cells with high-dose chemotherapy and then re-introducing healthy donor stem cells into the body. The new stem cells can rebuild a healthy blood supply and immune system.
Even though these therapies are the treatment of choice for kids with JMML, the disease remains difficult to cure. As a result, researchers are looking into the use of molecular-targeted therapies (medications that block the expansion of cancer cells by disrupting certain molecules or proteins needed for growth), which also may be an effective treatment.
Being told that your child has cancer can be a terrifying experience, and the stress of treating the disease can be overwhelming for any family.
Although you might feel like it at times, you're not alone. To find out about support that may be available to you or your child, talk to your doctor or a hospital social worker. Many resources are available that can help you get through this difficult time.
Reviewed by: Emi H. Caywood, MD
Date reviewed: March 2012