| Literature DB >> 27549546 |
Benedetto Del Forno1, Carlo Zingaro2, Enza Di Palma2, Filippo Capestro2, Giuseppe Rescigno2, Lucia Torracca2.
Abstract
Primary cardiac paragangliomas are extremely rare. Recently this neoplasm has been associated with a familiar syndrome as a result of mutation of genes that encode proteins in the mitochondrial complex II. We report a case of a 46-year-old woman having cases of vertebral paraganglioma in her family showing an unusual anatomic and clinical presentation of cardiac paraganglioma and expressing a genetic mutation never associated before with cardiac localization of this neoplasm.Entities:
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Year: 2016 PMID: 27549546 DOI: 10.1016/j.athoracsur.2016.01.072
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330