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]
Affiliations
- 1 Serviço de Cardiologia, Hospital Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal. Electronic address: milan.satendra@gmail.com.
- 2 Serviço de Medicina, Hospital Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal.
- 3 Serviço de Cardiologia, Hospital Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal.
- 4 Serviço de Cirurgia II, Hospital Santa Maria, Centro Hospitalar Lisboa Norte, Lisboa, Portugal.
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.
Copyright © 2013 Sociedade Portuguesa de Cardiologia. Published by Elsevier España. All rights reserved.
MeSH terms
-
Adrenal Gland Neoplasms / blood
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Adrenal Gland Neoplasms / complications*
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Adult
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Cardiomyopathy, Dilated / blood
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Cardiomyopathy, Dilated / etiology*
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Catecholamines / blood
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Humans
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Male
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Pheochromocytoma / blood
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Pheochromocytoma / complications*