Literature DB >> 27549546

Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation.

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.
Copyright © 2016 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

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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


  2 in total

1.  Multimodality Imaging Evaluation of Primary Right Atrial Paraganglioma: A Case Report and Literature Review.

Authors:  Wen-Peng Huang; Ge Gao; Zhao Chen; Yong-Kang Qiu; Jian-Bo Gao; Lei Kang
Journal:  Front Med (Lausanne)       Date:  2022-06-30

2.  Unusual cardiac paraganglioma mimicking an atypical carcinoid tumor of the lung.

Authors:  Dean Spencer; Mark Evans; Beverly Wang; J Lawrence Delrosario; Timmy Cheng; Jeffrey Milliken
Journal:  J Thorac Dis       Date:  2018-01       Impact factor: 2.895

  2 in total

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