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一例罕见的先天性心脏畸形并存病例成功进行主动脉根部置换和分流闭合：二叶式主动脉瓣合并主动脉根部扩张、单冠状动脉和卵圆孔未闭。

Successful aortic root replacement and shunt closure in a case with rare coexistence of congenital cardiac malformations: bicuspid aortic valve with annuloaortic ectasia, single coronary artery, and patent foramen ovale.

作者信息

Egashira Toru, Shimizu Hideyuki, Yamada Yoshitake, Fukuda Keiichi

机构信息

Department of Cardiology, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku, Tokyo, 160-8582, Japan,

出版信息

Int J Cardiovasc Imaging. 2014 Oct;30(7):1267-8. doi: 10.1007/s10554-014-0458-0. Epub 2014 Jun 11.

DOI:10.1007/s10554-014-0458-0
PMID:24916464
Abstract

This is the first report of rare simultaneous complication of three cardiac malformations: bicuspid aortic valve with annuloaortic ectasia, single coronary artery, and patent foramen ovale. We successfully operated to replace the aortic valve and ascending aorta, and to close the patent foramen ovale.

摘要

这是关于三种心脏畸形罕见同时并发的首次报告

二叶式主动脉瓣伴主动脉瓣环扩张、单支冠状动脉和卵圆孔未闭。我们成功实施了手术，置换主动脉瓣和升主动脉，并闭合卵圆孔未闭。

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Successful aortic root replacement and shunt closure in a case with rare coexistence of congenital cardiac malformations: bicuspid aortic valve with annuloaortic ectasia, single coronary artery, and patent foramen ovale.一例罕见的先天性心脏畸形并存病例成功进行主动脉根部置换和分流闭合：二叶式主动脉瓣合并主动脉根部扩张、单冠状动脉和卵圆孔未闭。
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J Cardiothorac Surg. 2016 Oct 24;11(1):150. doi: 10.1186/s13019-016-0542-8.

本文引用的文献

1
Isolated single coronary artery: diagnosis, angiographic classification, and clinical significance.孤立性单冠状动脉：诊断、血管造影分类及临床意义。
Radiology. 1979 Jan;130(1):39-47. doi: 10.1148/130.1.39.