| Literature DB >> 28398370 |
Davide Muratori1, Patrizia Pedrotti1, Matteo Baroni1, Armando Belloni2, Giuseppina Quattrocchi1, Angela Milazzo1, Cristina Giannattasio3, Alberto Roghi1.
Abstract
Pheochromocytoma is a rare tumor, usually benign, potentially lethal in case of crisis with acute release of catecholamines. The heart is a target and the clinical presentation can mimic various cardiac conditions, thus rendering diagnosis elusive. Cardiac magnetic resonance is a valuable non-invasive diagnostic tool for the evaluation of cardiomyopathies; it allows the identification of catecholamine-induced myocarditis pattern and, in some cases, it can detect the primary tumor. The definitive treatment of pheochromocytoma is surgical, while the acute crisis may require mechanical support to circulation. We here report a case of pheochromocytoma in a 25-year-old man complicated by catecholamine-induced myocarditis and heart failure.Entities:
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Year: 2017 PMID: 28398370 DOI: 10.1714/2663.27302
Source DB: PubMed Journal: G Ital Cardiol (Rome) ISSN: 1827-6806