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Pheochromocytoma

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Definition: A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298)  benign or malignant; coord IM with usually ADRENAL GLAND NEOPLASMS (IM)   
See Also Multiple Endocrine Neoplasia Type 2a; Multiple Endocrine Neoplasia Type 2b
Other names Pheochromocytoma, Extra-Adrenal; Pheochromocytomas, Extra-Adrenal; Pheochromocytomas; Pheochromocytoma, Extra Adrenal; Extra-Adrenal Pheochromocytomas; Extra-Adrenal Pheochromocytoma

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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