Literature DB >> 19559176

Aortic valve replacement in a patient with Osler-Rendu-Weber disease.

Mariano N Benzadón1, Juan Pablo Costabel, Alberto Alves de Lima, Fernando Botto, María Ester Aris Cancela, Guillermo Vaccarino, Marcelo Trivi, Daniel Navia.   

Abstract

Osler-Rendu-Weber (hereditary hemorrhagic telangiectasia) disease is an uncommon disease characterized by the presence of abnormal telangiectasias and arteriovenous malformations that cause recurrent episodes of bleeding. We present a patient with Osler-Rendu-Weber disease, with a history of multiple major bleeding events and severe aortic valve stenosis, who underwent aortic valve replacement. Unexpectedly, the postoperative course was uneventful, and there was no untoward bleeding in the early or in the late postoperative follow-up.

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Year:  2009        PMID: 19559176     DOI: 10.1016/j.athoracsur.2009.02.014

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  2 in total

1.  Endocarditis after transfemoral aortic valve implantation in a patient with Osler-Weber-Rendu syndrome.

Authors:  Alessandro Castiglioni; Alberto Pozzoli; Francesco Maisano; Ottavio Alfieri
Journal:  Interact Cardiovasc Thorac Surg       Date:  2012-06-12

2.  Redo cardiac surgery for active prosthetic valve endocarditis associated with hereditary hemorrhagic telangiectasia: report of a case.

Authors:  Yuki Nakamura; Fumiaki Shikata; Masahiro Ryugo; Toru Okamura; Takumi Yasugi; Hironori Izutani
Journal:  Surg Today       Date:  2014-03-20       Impact factor: 2.549

  2 in total

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