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双孔二尖瓣:孤立性重度先天性二尖瓣反流的罕见病因。

Double orifice mitral valve: A rare cause of isolated severe congenital mitral regurgitation.

作者信息

Pratap Himanshu, Gupta Amol, Acharya Pradipta Kumar, Mahajan Viresh

机构信息

Department of Pediatric Cardiac Surgery, Asian Institute of Medical Sciences, Faridabad, Haryana, India.

Department of Pediatric Cardiology, Asian Institute of Medical Sciences, Faridabad, Haryana, India.

出版信息

Ann Pediatr Cardiol. 2020 Apr-Jun;13(2):174-176. doi: 10.4103/apc.APC_133_19. Epub 2020 Feb 14.

Abstract

Double orifice mitral valve (DOMV) is a rare congenital anomaly of the mitral valve apparatus consisting of an accessory bridge of fibrous tissue, which partially or completely divides the mitral valve into two orifices. It usually occurs as an associated lesion. Encountering a DOMV as an isolated finding meriting intervention is indeed rare. We, here, report a case of "complete bridging type DOMV" occurring as an isolated entity and presenting as severe congenital MR requiring surgery.

摘要

双孔二尖瓣(DOMV)是一种罕见的二尖瓣装置先天性异常,由纤维组织的副桥组成,该副桥将二尖瓣部分或完全分为两个孔。它通常作为一种相关病变出现。作为值得干预的孤立发现遇到DOMV确实很少见。在此,我们报告一例“完全桥接型DOMV”作为孤立实体出现,并表现为需要手术的严重先天性二尖瓣反流的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bebf/7331838/d14c3d5fc1cd/APC-13-174-g001.jpg

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