Left atrioventricular valve replacement in a patient with hereditary haemorrhagic telangiectasia

Yasunori Iida, Naritaka Kimura, Akinori Hirano, Hideyuki Shimizu

研究成果: Article査読

抄録

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.

本文言語English
ページ(範囲)327-328
ページ数2
ジャーナルInteractive cardiovascular and thoracic surgery
25
2
DOI
出版ステータスPublished - 2017 8 1

ASJC Scopus subject areas

  • 外科
  • 呼吸器内科
  • 循環器および心血管医学

フィンガープリント

「Left atrioventricular valve replacement in a patient with hereditary haemorrhagic telangiectasia」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル