Pheochromocytoma

What is a pheochromocytoma?

A pheochromocytoma is an adrenal gland tumor that secretes epinephrine and norepinephrine hormones. These hormones are responsible for regulating heart rate and blood pressure, among other functions. Pheochromocytomas occur most frequently in young to middle-aged adults between the ages of 30 and 60. Ten percent of individuals affected are children who usually develop symptoms between the ages of 6 and 14.

What causes pheochromocytomas?

The causes of pheochromocytoma are multifactorial, meaning "many factors" contribute to the cause of the condition. In most cases, both genetic and environmental factors play a role. The condition can occur alone or in combination with other disorders. The following are the most common disorders associated with pheochromocytoma:

neurofibromatosis
Von Hippel-Lindau disease
multiple endocrine neoplasia (MEN) syndromes
tuberous sclerosis
Sturge-Weber syndrome
a taxia-telangiectasia

What are the symptoms of pheochromocytoma?

The most common symptom of pheochromocytoma is high blood pressure, which is sometimes extreme. Each child may experience symptoms differently. Other symptoms may include:

rapid pulse
heart palpitations
headache
dizziness
poor weight gain despite good appetite
growth failure
nausea
vomiting
abdominal pain
pale skin
clammy skin
sweating

The symptoms of pheochromocytoma may resemble other problems or medical conditions. Always consult your child's physician for a diagnosis.

How is pheochromocytoma diagnosed?

In addition to a complete medical history and physical examination, diagnostic procedures for pheochromocytoma may include:

blood and urine tests (to measure hormone levels)
computed tomography scan (Also called a CT or CAT scan.) - a diagnostic imaging procedure that uses a combination of x-rays and computer technology to produce cross-sectional images (often called slices), both horizontally and vertically, of the body. A CT scan shows detailed images of any part of the body, including the bones, muscles, fat, and organs. CT scans are more detailed than general x-rays.
radioisotope scan - uses radioactive substances introduced into the body to create an image of the functioning adrenal gland.

Treatment for pheochromocytoma:

Specific treatment for pheochromocytoma will be determined by your child's physician based on:

your child's age, overall health, and medical history
the extent of the disease
the type of disease
your child's tolerance for specific medications, procedures, or therapies
expectations for the course of the disease
your opinion or preference

Treatment for pheochromocytoma usually includes removing the tumor. Before removing the tumor, however, your child's physician may prescribe medications to control high blood pressure. In children, there may be multiple tumors. An extensive evaluation to locate them will be required before surgery.

Continuous medical follow-up may be required to monitor the development of future tumors.

Family members may also want to consider testing to rule out the presence of the tumors, as genetics does appear to play a role in some cases.

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