A pregnant woman with Ebstein's anomaly. A case report.

F Gültekin, E Baskin, A Gökalp, K Dogan
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Abstract

Ebstein's anomaly is characterised by downward displacement of the tricuspid valve into the right ventricle. The most deformed leaflets are the septal and mural ones. The abnormally situated tricuspid orifice produces a portion of the right ventricle lying between the atrioventricular ring and the origin of the valve. This proximal segment is atrialized. Commonly associated anatomical defects include a atrial septal second defect, a ventricular septal defect, pulmonary stenosis or atresia, and mitral valve prolapse. An accessory conduction pathway (Wolf-Parkinson White syndrome) was found in this malformation. It is thought that this malformation is due to a direct teratogenic effect of lithium on the atrioventricular junction. Ebstein's anomaly can be accurately identified by echocardiography and angiography.

一个患有Ebstein异常的孕妇。一份病例报告。
Ebstein畸形的特征是三尖瓣向下移位进入右心室。最畸形的小叶是鼻中隔和壁叶。位于异常位置的三尖瓣口产生了位于房室环和瓣膜起源之间的一部分右心室。这段近端是心房化的。常见的相关解剖缺陷包括房间隔第二缺损、室间隔缺损、肺动脉狭窄或闭锁以及二尖瓣脱垂。在该畸形中发现了副传导通路(Wolf-Parkinson - White综合征)。据认为,这种畸形是由于锂对房室连接处的直接致畸作用。Ebstein异常可通过超声心动图和血管造影准确识别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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