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KEY POINTS
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A pheochromocytoma is a rare kind of tumor in one or both adrenal glands. Rarely, tumors may also be in other parts of the body.
Your adrenal glands are located near the top of each kidney. They make several different hormones that help control body functions such as blood pressure, and the levels of water, salt, and minerals in your body.
The tumor makes too many of the hormones that increase blood pressure and heart rate. The high level of these hormones can cause strokes, sudden death, heart attacks, abnormal heart rhythm, or heart failure.
Most pheochromocytomas are benign. Benign tumors are not cancer and do not spread to other parts of your body.
The cause of pheochromocytoma is not known. It may be inherited, which means that it is passed from parents to children through their genes. Genes are inside each cell of your body. They contain the information that tells your body how to develop and work.
The tumor may not cause any symptoms. If you do have symptoms, they may happen several times a day or only once a month. The symptoms may last only a few seconds or for hours. The most common symptoms that happen along with high blood pressure include:
Symptoms usually come and go. You may have symptoms several times a day or weeks apart. These symptoms will happen more often and will get worse as the tumor grows.
Your healthcare provider will ask about your symptoms and medical history and examine you. Tests may include:
Surgery to remove all or part of one or both adrenal glands is the most common treatment. To prepare for surgery, you will be treated for at least 7 days with medicines that block the effects of the substance made by the tumor. You may be in the hospital for a week or two. If both adrenal glands were removed, you may need to take medicines to replace the hormones made by the glands.
A few pheochromocytomas are cancer. If you have this type of tumor, possible treatments include:
Your healthcare provider will schedule checkups for several months after treatment.
Most people feel better after the tumor is removed. However, sometimes the tumor comes back.
Follow the full course of treatment prescribed by your healthcare provider. Ask your provider:
Make sure you know when you should come back for a checkup. Keep all appointments for provider visits or tests.
Because pheochromocytoma may be inherited, your healthcare provider may advise you to have genetic tests or genetic counseling.