Pediatric Anemia (aplastic)

What is aplastic anemia?

Aplastic anemia occurs when the bone marrow produces too few of all types of blood cells: red cells, white cells, and platelets. A reduced number of red blood cells causes the red cell number and hemoglobin (a type of protein in the red blood cells that carries oxygen to the tissues of the body) to drop. A reduced number of white blood cells causes the patient to be susceptible to infection. A reduced number of platelets can cause the blood not to clot the way it should.

What causes aplastic anemia?

Aplastic anemia in children has multiple causes. Some of these causes are idiopathic, meaning they occur sporadically for no known reason. Other causes are secondary, resulting from a previous illness or disorder. Very often there is an immunological dysfunction (immune system problem) or malignant (cancerous) change in the cells.

Many childhood cases of aplastic anemia occur sporadically for no known reason. Acquired causes, however, may include:

• History of specific infectious diseases, such as hepatitis, Epstein-Barr virus (EBV), cytomegalovirus (CMV), parvovirus B19, or human immunodeficiency virus (HIV)
• History of taking certain medications
• Exposure to certain toxins, such as heavy metals
• Exposure to radiation
• History of an autoimmune disease, such as lupus
• A developing acute lymphocytic leukemia 

Children may also inherit a disorder that predisposes them to developing aplastic anemia. Some disorders that are known to predispose a child to aplastic anemia include:

• Fanconi anemia
• Dyskeratosis congenita
• Shwachman-Diamond syndrome
• Reticular dysgenesis
• Amegakaryocytic thrombocytopenia
• Familial aplastic anemias

What are the symptoms of aplastic anemia?

The following are the most common symptoms of aplastic anemia. However, each child may experience symptoms differently. Symptoms may include:

• Headache
• Dizziness
• Nausea
• Shortness of breath
• Bruising
• Lack of energy or tiring easily (fatigue)
• Abnormal paleness or lack of color of the skin
• Blood in stool
• Nosebleeds
• Bleeding gums
• Fevers
• Sinus tenderness
• Enlarged liver or spleen
• Oral thrush (white patches on a red, moist, swollen surface, occurring anywhere in the mouth)

The symptoms of aplastic anemia may resemble other blood disorders or medical problems. Always consult your child's doctor for a diagnosis.

How is aplastic anemia diagnosed?

In addition to a complete medical history and physical examination of your child, diagnostic procedures for aplastic anemia may include:

• Blood tests
• Bone marrow aspiration and/or biopsy

A procedure that involves taking a small amount of bone marrow fluid (aspiration) and/or solid bone marrow tissue called a core biopsy, usually from the hip bones, to be examined for the number, size, and maturity of blood cells and/or abnormal cells. In aplastic anemia typically the marrow is replaced by fat.

Treatment for aplastic anemia

Specific treatment for aplastic anemia will be determined by your child's doctor based on:

• Your child's age, overall health, and medical history
• The extent of the anemia
• Cause of the anemia
• Your child's tolerance for specific medications, procedures, or therapies
• Expectations for the course of the anemia
• Your opinion or preference

Aplastic anemia is a serious illness and treatment usually depends on the underlying cause. For certain causes, recovery can be expected after treatment; however, relapses can occur. To treat the low blood counts, initial treatment is usually supportive, meaning that it is necessary to treat the symptoms but not possible to cure the disease. Supportive therapy may include:

Activities which put children with aplastic anemia at risk for infection or bleeding should be avoided. These activities include things like the following:

If a child has a relapse of aplastic anemia, additional treatment (including a possible bone marrow transplant) may be necessary.