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Rev Port Cardiol ; 33(3): 177.e1-6, 2014 Mar.
Article in English, Portuguese | MEDLINE | ID: mdl-24684896

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.


Subject(s)
Adrenal Gland Neoplasms/complications , Cardiomyopathy, Dilated/etiology , Pheochromocytoma/complications , Adrenal Gland Neoplasms/blood , Adult , Cardiomyopathy, Dilated/blood , Catecholamines/blood , Humans , Male , Pheochromocytoma/blood
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