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.
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:
- Von Hippel-Lindau disease
- multiple endocrine neoplasia (MEN) syndromes
- tuberous sclerosis
- Sturge-Weber syndrome
- a taxia-telangiectasia
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
- poor weight gain despite good appetite
- growth failure
- abdominal pain
- pale skin
- clammy skin
The symptoms of pheochromocytoma may resemble other problems or medical conditions. Always consult your child's physician for a diagnosis.
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.
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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