Ebstein异常、左心室不致密和gerbode样缺陷三联征(胎儿诊断和新生儿病程)。

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2021-11-11 eCollection Date: 2021-01-01 DOI:10.1155/2021/9969588
Mohammad Mehdi, Snigdha Bhatia, Mehul Patel, Ashraf Aly
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引用次数: 1

摘要

Ebstein畸形的特征是三尖瓣的间隔和后小叶的顶端移位,右心室(RV)心房化。它通常与其他心脏缺陷有关,包括左心室不致密。我们描述了一例产前诊断的Ebstein异常与左心室不致密和左心室与右心室心房部分之间的间隔缺损(gerbode样缺损)有关。由于严重的右室发育不全和右室流出道梗阻,患者接受了改良的Blalock-Taussig分流术和Glenn手术。患者对这两种手术都能耐受,并且在临床上表现良好,预计Fontan手术将用于单心室姑息治疗。
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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Ebstein's Anomaly, Left Ventricular Noncompaction and Gerbode-Like Defect Triad (Fetal Diagnosis and Neonatal Course).

Ebstein's anomaly is characterized by the apical displacement of the septal and posterior leaflets of the tricuspid valve with atrialization of the right ventricle (RV). It is commonly associated with other heart defects including left ventricular noncompaction. We describe a case of prenatally diagnosed Ebstein's anomaly in association with left ventricular noncompaction and a septal defect between the left ventricle and the atrialized portion of the RV (Gerbode-like defect). The patient underwent a modified Blalock-Taussig shunt followed by Glenn procedure because of severe RV hypoplasia and RV outflow tract obstruction. The patient tolerated both procedures and is doing clinically well in anticipation of Fontan procedure for single ventricle palliation.

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自引率
11.10%
发文量
48
审稿时长
13 weeks
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