Neuroblastoma is a malignant (cancerous)
Neuroblastoma can occur in many areas of the body. It develops from the tissues that form the sympathetic nervous system. This is the part of the nervous system that controls body functions, such as
Most neuroblastomas begin in the abdomen in the adrenal gland or next to the spinal cord, or in the chest. Neuroblastomas can spread to the bones. These include the face, skull, pelvis, shoulders, arms, and legs. It can also spread to the bone marrow, liver, lymph nodes, skin, and around the eyes (orbits).
The cause of the tumor is not known. Neuroblastoma is commonly diagnosed in children before age 5. Each year there are around 700 new cases in the United States. The disorder occurs in approximately 1 out of 100,000 children and is slightly more common in boys.
In most patients, the tumor has spread when it is first diagnosed.
The first symptoms are usually fever, a general sick feeling (
Other symptoms depend on the site of the tumor, and may include:
Bone pain or tenderness(if the cancer has spread to the bones)
- Difficulty breathing or a chronic cough (if the cancer has spread to the chest)
- Enlarged abdomen (from a large tumor or excess fluid)
- Flushed, red skin
- Pale skin and bluish color around the eyes
- Profuse sweating
- Rapid heart rate (
Brain and nervous system problems may include:
- Inability to empty the bladder
- Loss of movement (
paralysis) of the hips, legs, or feet (lower extremities)
- Problems with balance
Uncontrolled eye movementsor leg and feet movements (called opsoclonus-myoconus syndrome, or “dancing eyes and dancing feet”)
Exams and Tests
Signs vary, depending on the location of the tumor.
Examination of the abdomen with the hands (
palpation) may reveal a lump or mass.
The liver may be enlarged, if the tumor has spread to the liver.
Adrenal gland tumors can cause high blood pressure and a fast heart rate.
Lymph nodes may be swollen.
X-ray or other imaging tests are done to locate the main (primary) tumor and to see where it has spread. These include:
- Bone x-rays
Chest x-ray CT scanof chest and abdomen MRI scanof chest and abdomen
Other tests include:
Biopsyof tumor Bone marrow biopsy CBC(complete blood count) showing anemiaor other abnormality
- Coagulation studies, erythrocyte sedimentation rate (
- Hormone tests (blood tests to check levels of hormones such as
catecholamines) MIBG scan Urine 24-hour testfor catecholamines, homovanillic acid (HVA), and vanillymandelic acid (VMA)
Treatment depends on:
Location of the tumor
How much and where the tumor has spread
The patient’s age
In certain cases, surgery alone is enough. Often, though, other therapies are needed. Anticancer medicines (
High-dose chemotherapy, followed by autologous
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Outcome varies. In very young children, the tumor may go away on its own, without treatment. Or, the tissues of the tumor may mature and develop into a non-cancerous (benign) tumor called a
Response to treatment also varies. Treatment is often successful if the cancer has not spread. If it has spread, neuroblastoma is harder to cure. Younger children often do better than older children.
Children treated for neuroblastoma may be at risk of getting a second, different cancer in the future.
- Spread (
metastasis) of the tumor
- Damage and loss of function of involved organ(s)
When to Contact a Medical Professional
Call your health care provider if your child has symptoms of neuroblastoma. Early diagnosis and treatment improves the chance of a good outcome.