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What type of cancer is pheochromocytoma? Pheochromocytoma and paraganglioma are rare tumors that come from the same type of tissue. Pheochromocytoma is a rare tumor that forms in the adrenal medulla (the center of the adrenal gland). Certain inherited disorders and changes in certain genes increase the risk of pheochromocytoma or paraganglioma.
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What type of cancer is paraganglioma? Paraganglioma. A paraganglioma is a rare tumor that begins in certain nerve cells that are dispersed throughout the body. This tumor can affect people of any age but most often shows up between the ages of 30 and 50. The tumor is often slow growing and noncancerous (benign).
Which signs and symptoms are consistent with pheochromocytoma? Signs and symptoms of pheochromocytomas often include: High blood pressure. Heavy sweating. Headache. Rapid heartbeat (tachycardia) Tremors. Paleness in the face (pallor) Shortness of breath (dyspnea)
What type of cancer is pheochromocytoma? Pheochromocytoma and paraganglioma are rare tumors that come from the same type of tissue. Pheochromocytoma is a rare tumor that forms in the adrenal medulla (the center of the adrenal gland). Certain inherited disorders and changes in certain genes increase the risk of pheochromocytoma or paraganglioma.
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