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先天性三尖瓣口无保护:与肺动脉闭锁及完整室间隔相关时与埃布斯坦畸形的鉴别。

Congenitally unguarded tricuspid orifice: its differentiation from Ebstein's malformation in association with pulmonary atresia and intact ventricular septum.

作者信息

Anderson R H, Silverman N H, Zuberbuhler J R

机构信息

Division of Pediatric Cardiology, Children's Hospital of Pittsburgh, Pennsylvania.

出版信息

Pediatr Cardiol. 1990 Apr;11(2):86-90. doi: 10.1007/BF02239568.

Abstract

Dysplasia of the leaflets is a well-known integral part of Ebstein's malformation. It is less well-recognized that occasionally the septal leaflet may be completely absent and not simply displaced from its usual annular attachment. This may make it difficult to differentiate by echocardiography between Ebstein's malformation and the rare lesion in which the tricuspid orifice is completely devoid of leaflet tissue ("congenitally unguarded orifice"). A neonatal case is described in which a partially unguarded orifice was present in association with pulmonary atresia and intact ventricular septum but misdiagnosed as Ebstein's malformation. In addition we reviewed the morphologic features of all 46 cases of pulmonary atresia and intact septum in the Cardiopathological Collection of the Children's Hospital of Pittsburgh: 17 also had Ebstein's malformation, while three had a congenitally unguarded tricuspid orifice. We found that the differential diagnosis occurred when the right ventricle was dilated rather than being a hypoplastic cavity, as was a feature of all the cases with unguarded orifice and five of those with Ebstein's malformation. The difference between the lesions is best demonstrated by examining the mural leaflet of the valve, which is absent when the orifice is unguarded but displaced in association with Ebstein's malformation. This feature should be recognizable by cross-sectional echocardiography. We have confirmed previous studies that dilatation of the chambers of the right heart indicates a very poor prognosis in cases with pulmonary atresia and an intact ventricular septum.

摘要

瓣叶发育异常是埃布斯坦畸形(Ebstein畸形)的一个众所周知的重要组成部分。但鲜为人知的是,偶尔间隔瓣叶可能完全缺失,而不仅仅是从其通常的瓣环附着处移位。这可能使得通过超声心动图难以区分埃布斯坦畸形与罕见的三尖瓣口完全没有瓣叶组织的病变(“先天性无瓣口”)。本文描述了1例新生儿病例,该病例存在部分无瓣口并伴有肺动脉闭锁及室间隔完整,但被误诊为埃布斯坦畸形。此外,我们回顾了匹兹堡儿童医院心脏病理收藏中所有46例肺动脉闭锁及室间隔完整病例的形态学特征:其中17例还合并有埃布斯坦畸形,3例有先天性无瓣三尖瓣口。我们发现,当右心室扩张而不是发育不良时,就会出现鉴别诊断问题,这是所有无瓣口病例以及5例埃布斯坦畸形病例的一个特征。通过检查瓣膜的壁叶可以最好地显示病变之间的差异,当瓣口无瓣时壁叶缺失,而在埃布斯坦畸形时壁叶移位。这一特征应该可以通过横断面超声心动图识别。我们证实了先前的研究结果,即右心腔扩张表明肺动脉闭锁及室间隔完整病例的预后非常差。

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