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主动脉缩窄合并肺动脉瓣缺如综合征及室间隔缺损。

Coarctation of the aorta in the syndrome of absent pulmonary valve with ventricular septal defect.

作者信息

Hofbeck M, Röckelein G, Singer H, Rein J, Gittenberger-de Groot A C

机构信息

Paediatric Department, University Erlangen-Nuremberg, FRG.

出版信息

Pediatr Cardiol. 1990 Jul;11(3):159-63. doi: 10.1007/BF02238849.

Abstract

The case of a male child is reported in which the syndrome of absent pulmonary valve and ventricular septal defect was associated with anomalous drainage of the right superior pulmonary vein into the superior vena cava, atrial septal defect, a right aortic arch, and an aortic isthmic coarctation. The combination of aortic coarctation with a high degree of right-ventricular outflow obstruction has not been reported so far in the literature. This case shows that there is no proof of aplasia of the ductus arteriosus in the syndrome of absent pulmonary valve and ventricular septal defect. Most likely, there is an early involution of the ductus arteriosus; persistence of the ductus arteriosus would not be compatible with fetal survival.

摘要

报道了一名男童病例,该病例中肺动脉瓣缺如和室间隔缺损综合征与右上肺静脉异常引流至上腔静脉、房间隔缺损、右位主动脉弓及主动脉峡部缩窄相关。主动脉缩窄与高度右心室流出道梗阻并存的情况,目前文献中尚未见报道。该病例表明,肺动脉瓣缺如和室间隔缺损综合征中并无动脉导管发育不全的证据。很可能动脉导管早期就已退化;动脉导管持续存在与胎儿存活不相符。

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