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先天性三尖瓣病变谱:从 Ebstein 畸形到发育不良。

The Congenital Tricuspid Valve Spectrum: From Ebstein to Dysplasia.

机构信息

Department of Cardiovascular Surgery, 4352Mayo Clinic, Rochester, MN, USA.

Division of Pediatric Cardiology, 4352Mayo Clinic, Rochester, MN, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2020 Nov;11(6):783-791. doi: 10.1177/2150135120949235.

Abstract

Ebstein anomaly has a breadth of presentations, including "typical" and "atypical," and can be confused with congenital tricuspid dysplasia. We summarize how to differentiate within this spectrum of disease. Both typical and atypical Ebstein have an underlying failure of delamination, but atypical Ebstein does not have ≥8mm/m apical septal leaflet displacement. In congenital tricuspid dysplasia, delamination is normal, while the leaflets and subvalvar apparatus are abnormal. To summarize, the sine qua non feature of Ebstein anomaly, present in both typical and atypical, is the failure of delamination. These are distinct from congenital tricuspid valve dysplasia in which the pathology is in the leaflet itself.

摘要

Ebstein 畸形有多种表现形式,包括“典型”和“非典型”,并可能与先天性三尖瓣发育不良相混淆。我们总结了如何在这一疾病谱中进行鉴别。典型和非典型 Ebstein 畸形都存在内在的分层失败,但非典型 Ebstein 畸形的瓣叶无≥8mm/m 的 apical septal 叶位移。在先天性三尖瓣发育不良中,分层正常,而瓣叶和瓣下装置异常。总之,Ebstein 畸形的必要特征,无论是典型还是非典型,都是分层失败。这与瓣叶本身存在病变的先天性三尖瓣瓣膜发育不良不同。

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