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先天性矫正型大动脉转位合并肺动脉闭锁及室间隔完整

Congenitally corrected transposition with pulmonary atresia and intact ventricular septum.

作者信息

Patel C R, Spector M L, Zahka K G

机构信息

Department of Pediatrics, Rainbow Babies and Childrens Hospital, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

出版信息

Cardiol Young. 2000 May;10(3):268-70. doi: 10.1017/s1047951100009227.

DOI:10.1017/s1047951100009227
PMID:10824910
Abstract

We describe a patient with the rare association of the heart in the left chest, congenitally corrected transposition, pulmonary atresia and an intact ventricular septum. There were associated fistulous communications between the morphologically left ventricle and the coronary arteries. Diagnosis was made by echocardiography, and subsequently confirmed by cardiac catheterization.

摘要

我们描述了一名患者,其存在心脏位于左胸、先天性矫正性大动脉转位、肺动脉闭锁及室间隔完整这种罕见的关联情况。形态学上的左心室与冠状动脉之间存在相关的瘘管交通。通过超声心动图做出诊断,随后经心导管检查得以证实。

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引用本文的文献

1
Pulmonary atresia with intact ventricular septum associated with congenitally corrected transposition.室间隔完整的肺动脉闭锁合并先天性矫正型大动脉转位。
Pediatr Cardiol. 2006 Nov-Dec;27(6):741-5. doi: 10.1007/s00246-005-1195-x.