Literature DB >> 20852328

Right atrial lipoma in patient with Cowden syndrome.

Fabrizio Ceresa1, Graziella Calarco, Enrico Franzì, Francesco Patanè.   

Abstract

Primary cardiac tumors are rarest form of cancer and the lipoma represent about 8% of these tumors. Cowden disease is a rare autosomal dominant disorder, associated to a germline mutation of the PTEN gene, characterized by multiple hamartomas and an increased risk of breast, thyroid and endometrial carcinomas. For the first time, we describe a right atrial lipoma in a patient affected by Cowden syndrome. The patient suffered of some episodes of atrial flutter. The echocardiogram showed a cardiac mass, suggestive of lipoma with cardiac magnetic resonance images. Right atrial mass was completely resected and the histological examination confirmed the diagnosis of lipoma. The patient was discharged from hospital without any complications.

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Year:  2010        PMID: 20852328     DOI: 10.1510/icvts.2010.245001

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  5 in total

1.  Left atrial cavernous haemangioma presenting with cardiac tamponade in a patient with Cowden syndrome.

Authors:  Alexandra Drucker; Chong Zhou; Siven Seevanayagam; Laurence Weinberg
Journal:  BMJ Case Rep       Date:  2019-07-08

2.  Enlarging left atrial haemangioma in a patient with Cowden syndrome.

Authors:  Anthony Lamanna; Ruth P Lim; Lee Pheng Yap; Julian Maingard; Siven Seevenayagam
Journal:  BMJ Case Rep       Date:  2019-07-27

3.  A rare case of a intracardiac lipoma.

Authors:  Sarabjeet Singh; Mukesh Singh; Daniela Kovacs; Daniel Benatar; Sandeep Khosla; Harpreet Singh
Journal:  Int J Surg Case Rep       Date:  2015-02-20

4.  An asymptomatic right atrial intramyocardial lipoma: a management dilemma.

Authors:  Haiyong Wang; Jiangwei Hu; Xiaolin Sun; Pingshan Wang; Zhenzong Du
Journal:  World J Surg Oncol       Date:  2015-02-06       Impact factor: 2.754

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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