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主动脉缩窄与法洛四联症及肺动脉闭锁并存。

Coarctation co-existing with tetralogy of Fallot and pulmonary atresia.

作者信息

Yip R C, Deekollu D, Arnold R

机构信息

Department of Cardiology, Alder Hey Hospital, Royal Liverpool Children's Hospital, UK.

出版信息

Cardiol Young. 2001 Jan;11(1):88-90. doi: 10.1017/s1047951100012488.

Abstract

We describe the finding of unsuspected aortic coarctation, discovered by catheterisation at 4 months, in a neonate first daignosed on the fourth day of life as having tetralogy of Fallot with pulmonary atresia and major aorto-to-pulmonary collateral arteries. This previously unreported combination contravenes the established theory of patterns of flow during fetal life, and presented difficult issues in clinical management.

摘要

我们描述了一名新生儿的情况,该新生儿出生后第四天首次被诊断为法洛四联症合并肺动脉闭锁及主要的主动脉-肺动脉侧支动脉,4个月时通过心导管检查发现了此前未被怀疑的主动脉缩窄。这种先前未报道过的组合与已确立的胎儿期血流模式理论相悖,并在临床管理中带来了难题。

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