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对一名患有马凡综合征的儿童进行二尖瓣、主动脉瓣置换及冠状动脉移植并升主动脉置换术。

Replacement of the mitral valve, aortic valve, and ascending aorta with coronary transplantation in a child with the Marfan syndrome.

作者信息

Caves P K, Paneth M

出版信息

Thorax. 1972 Jan;27(1):58-65. doi: 10.1136/thx.27.1.58.

Abstract

A girl with the Marfan syndrome is described who developed mitral regurgitation, an aneurysm of the ascending aorta, and severe aortic regurgitation. Complete surgical correction required mitral valve, aortic valve, and ascending aorta replacement with transplantation of the origin of the coronary arteries. The cardiovascular complications of the Marfan syndrome are discussed and the previously described surgical techniques for dealing with aortic or mitral involvement are briefly reviewed. A simpler and safer method for replacement of the complete ascending aorta with coronary artery transplantation is described.

摘要

本文描述了一名患有马凡综合征的女孩,她出现了二尖瓣反流、升主动脉瘤和严重的主动脉瓣反流。完整的手术矫正需要进行二尖瓣、主动脉瓣置换以及升主动脉置换,并移植冠状动脉起始部。文中讨论了马凡综合征的心血管并发症,并简要回顾了先前描述的处理主动脉或二尖瓣受累的手术技术。本文还描述了一种更简单、更安全的冠状动脉移植置换完整升主动脉的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/559d/472463/78bd9f69e1c2/thorax00121-0065-a.jpg

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