Pheochromocytoma (patient information)

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Pheochromocytoma is a rare tumor of adrenal gland. It results in the release of excessive amounts of epinephrine and norepinephrine, hormones that control heart rate, metabolism, and blood pressure .

• Abdominal pain
• Chest pain
• Irritability
• Nervousness
• Pallor
• Palpitations
• Rapid heart rate
• Severe headache
• Sweating
• Weight loss

Other symptoms that can occur with this disease:

• Hand tremor
• High blood pressure
• Sleeping difficulty

Symptom attacks may occur at unpredictable intervals and usually last 15 to 20 minutes. The attacks may increase in frequency, length, and severity as the tumor grows.

Pheochromocytoma may occur as a single tumor or as more than one growth. It usually develops in the center (medulla) of one or both adrenal glands. Rarely, this kind of tumor occurs outside the adrenal gland, usually somewhere else in the abdomen.

Very few pheochromocytomas are cancerous.

The tumors may occur at any age, but they are most common from early to mid-adulthood.

Call your health care provider if:

• You have symptoms of pheochromocytoma
• You had a pheochromocytoma in the past and your symptoms return

The doctor will perform a physical exam. You may have high blood pressure, rapid heart rate, and fever during an attack of symptoms. Your vital signs can be normal at other times.

Tests include:

• Abdominal CT scan
• Adrenal biopsy
• Catecholamines blood test
• Glucose test
• Metanephrine blood test
• MIBG scintiscan
• MRI of abdomen
• Urine catecholamines

Treatment involves removing the tumor with surgery. It is important to stabilize blood pressure and pulse with medication before surgery. You may need to stay in the hospital with close monitoring of your vital signs.

After surgery, it is necessary to continually monitor all vital signs in an intensive care unit. When the tumor cannot be surgically removed, medication is needed to manage it. This usually requires a combination of medications to control the effects of the excessive hormones. Radiation therapy and chemotherapy have not been effective in curing this kind of tumor.

Patients diagnosed with pheochromocytoma should avoid using the following medications:

• Atomoxetine
• Metoclopramide
  If you have been diagnosed with pheochromocytoma, consult your physician before starting or stopping any of these medications.

Directions to Hospitals Treating Pheochromocytoma

Most patients who have noncancerous tumors that are removed with surgery are still alive after 5 years. The tumors come back in less than 10% of these patients. Levels of the hormones norepinephrine and epinephrine return to normal after surgery.

High blood pressure may not be cured in 25% of patients after surgery. However, standard treatments can usually control high blood pressure. In about 10% of people, the tumor may return.

http://www.nlm.nih.gov/medlineplus/ency/article/000340.htm