Left atrioventricular valve replacement in a patient with hereditary haemorrhagic telangiectasia

Yasunori Iida; Naritaka Kimura; Akinori Hirano; Hideyuki Shimizu

doi:10.1093/icvts/ivx062

Left atrioventricular valve replacement in a patient with hereditary haemorrhagic telangiectasia

Yasunori Iida, Naritaka Kimura, Akinori Hirano, Hideyuki Shimizu

Department of Surgery (Cardiovascular Surgery)

Research output: Contribution to journal › Article › peer-review

Abstract

Hereditary haemorrhagic telangiectasia, or Osler-Rendu-Weber disease, is characterized by multiple arteriovenous malformations and telangiectasia which develop in the brain, lungs or liver. We report the case of a patient who had severe left atrioventricular valve regurgitation with atrial fibrillation after atrioventricular septal defect repair in her childhood and was diagnosed as having hereditary haemorrhagic telangiectasia by chance. The patient underwent successful left atrioventricular valve replacement and maze operation. The postoperative course was uneventful without nose bleeding worsening.

Original language	English
Pages (from-to)	327-328
Number of pages	2
Journal	Interactive cardiovascular and thoracic surgery
Volume	25
Issue number	2
DOIs	https://doi.org/10.1093/icvts/ivx062
Publication status	Published - 2017 Aug 1

Keywords

Adult congenital surgery
Arrhythmia
Genetic disease
Valve surgery

ASJC Scopus subject areas

Surgery
Pulmonary and Respiratory Medicine
Cardiology and Cardiovascular Medicine

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10.1093/icvts/ivx062

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abstract = "Hereditary haemorrhagic telangiectasia, or Osler-Rendu-Weber disease, is characterized by multiple arteriovenous malformations and telangiectasia which develop in the brain, lungs or liver. We report the case of a patient who had severe left atrioventricular valve regurgitation with atrial fibrillation after atrioventricular septal defect repair in her childhood and was diagnosed as having hereditary haemorrhagic telangiectasia by chance. The patient underwent successful left atrioventricular valve replacement and maze operation. The postoperative course was uneventful without nose bleeding worsening.",

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AU - Shimizu, Hideyuki

N1 - Publisher Copyright: © VC The Author 2017.

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AB - Hereditary haemorrhagic telangiectasia, or Osler-Rendu-Weber disease, is characterized by multiple arteriovenous malformations and telangiectasia which develop in the brain, lungs or liver. We report the case of a patient who had severe left atrioventricular valve regurgitation with atrial fibrillation after atrioventricular septal defect repair in her childhood and was diagnosed as having hereditary haemorrhagic telangiectasia by chance. The patient underwent successful left atrioventricular valve replacement and maze operation. The postoperative course was uneventful without nose bleeding worsening.

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Left atrioventricular valve replacement in a patient with hereditary haemorrhagic telangiectasia

Abstract

Keywords

ASJC Scopus subject areas

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