Literature DB >> 17900919

Black cardiac paraganglioma in a multiple paraganglioma syndrome.

Fabio Miraldi1, Chiara Taffon, Michele Toscano, Antonio Barretta.   

Abstract

We describe a unique case of a patient with a 'pigmented' cardiac paraganglioma in a multiple paraganglioma syndrome. She was symptomatic for arrhythmias, hypertensive crises and dyspnoea due to a cardiac tumour, which was richly vascularised from the right coronary artery and was partially obstructing the right atrioventricular inflow. She was operated on, but the mass was not completely resectable due to its relationship with cardiac structures. The histological findings were paraganglioma with abundant, dark granular pigment. To our knowledge, pigment presence has never been cited in surgical cases of cardiac paragangliomas.

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Year:  2007        PMID: 17900919     DOI: 10.1016/j.ejcts.2007.08.026

Source DB:  PubMed          Journal:  Eur J Cardiothorac Surg        ISSN: 1010-7940            Impact factor:   4.191


  5 in total

Review 1.  Comprehensive review of evaluation and management of cardiac paragangliomas.

Authors:  Sri Harsha Tella; Abhishek Jha; David Taïeb; Keith A Horvath; Karel Pacak
Journal:  Heart       Date:  2020-05-22       Impact factor: 5.994

2.  Pigmented paraganglioma of the kidney: a case report.

Authors:  Ling Zhao; Jie Luo; Honglei Zhang; Jiping Da
Journal:  Diagn Pathol       Date:  2012-06-28       Impact factor: 2.644

3.  A rare case of extra-adrenal pheochromocytoma localized to the ovary and detected via abdominal computed tomography angiography.

Authors:  Hui Liu; Wen-Zheng Li; Xiao-Yi Wang; Yi-Gang Pei; Xue-Yin Long; Chang-Yong Chen; Yong-Bin Hu
Journal:  Oncol Lett       Date:  2014-11-20       Impact factor: 2.967

4.  Somatic RET mutation in a patient with pigmented adrenal pheochromocytoma.

Authors:  Nicole Maison; Esther Korpershoek; Graeme Eisenhofer; Mercedes Robledo; Ronald de Krijger; Felix Beuschlein
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2016-01-18

5.  Intracardiac tumor as a rare manifestation of genetic syndromes-presentation of a family with Gorlin syndrome and a literature review.

Authors:  Krzysztof Szczałuba; Ewa Makuła; Anna Piórecka-Makuła; Justyna Sicińska; Małgorzata Rydzanicz; Piotr Gasperowicz; Rafał Płoski; Bożena Werner
Journal:  J Appl Genet       Date:  2020-09-22       Impact factor: 3.240

  5 in total

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