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Pheochromocytoma history and symptoms

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]Mohammed Abdelwahed M.D[3]

Overview

Overview

The hallmarks of pheochromocytoma is recurrent episodes of sympathetic symptoms. The most common symptoms of pheochromocytoma include episodes of palpitations, sweating and headaches. Less common symptoms include cardiomypathy, episodic hypotension, symptoms of other multiple endocrine neoplasias associated diseases such as that of medullary thyroid cancer and hyperparathyroidism.

History and Symptoms

History and Symptoms

The hallmark of pheochromocytoma is recurrent episodes of palpitations, sweating, and headache.

History

Patients with pheochromocytoma may have a positive history of:

Common symptoms

Common symptoms of pheochromocytoma are secondary to sympathetic nervous system hyperactivity. Symptoms usually subside in less than one hour and they may include:

Less common symptoms

Less common symptoms of pheochromocytoma include:

References

  1. Bravo EL, Gifford RW (1993). “Pheochromocytoma”. Endocrinol Metab Clin North Am. 22 (2): 329–41. PMID 8325290.
  2. Kassim TA, Clarke DD, Mai VQ, Clyde PW, Mohamed Shakir KM (2008). “Catecholamine-induced cardiomyopathy”. Endocr Pract. 14 (9): 1137–49. doi:10.4158/EP.14.9.1137. PMID 19158054.
  3. Bravo EL (1994). “Evolving concepts in the pathophysiology, diagnosis, and treatment of pheochromocytoma”. Endocr Rev. 15 (3): 356–68. doi:10.1210/edrv-15-3-356. PMID 8076587.
  4. Walther MM, Reiter R, Keiser HR, Choyke PL, Venzon D, Hurley K; et al. (1999). “Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma”. J Urol. 162 (3 Pt 1): 659–64. PMID 10458336.

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