Reversible catecholamine-induced cardiomyopathy due to pheochromocytoma: case report

Rev Port Cardiol. 2014 Mar;33(3):177.e1-6. doi: 10.1016/j.repc.2013.09.011. Epub 2014 Mar 28.
[Article in English, Portuguese]

Abstract

Pheochromocytoma is a tumor originating from chromaffin tissue. It commonly presents with symptoms and signs of catecholamine excess, such as hypertension, tachycardia, headache and sweating. Cardiovascular manifestations include catecholamine-induced cardiomyopathy, which may present as severe left ventricular dysfunction and congestive heart failure. We report a case of pheochromocytoma which was diagnosed following investigation of dilated cardiomyopathy. We highlight the dramatic symptomatic improvement and reversal of cardiomyopathy, with recovery of left ventricular function after treatment.

Keywords: Cardiomyopathy; Catecholamines; Catecolaminas; Feocromocitoma; Heart failure; Insuficiência cardíaca; Miocardiopatia; Pheochromocytoma.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Gland Neoplasms / blood
  • Adrenal Gland Neoplasms / complications*
  • Adult
  • Cardiomyopathy, Dilated / blood
  • Cardiomyopathy, Dilated / etiology*
  • Catecholamines / blood
  • Humans
  • Male
  • Pheochromocytoma / blood
  • Pheochromocytoma / complications*

Substances

  • Catecholamines