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大动脉位置正常伴膈下完全性肺静脉异位连接梗阻的大动脉转位：1例接受解剖修复的罕见病例

A situs solitus transposition of great arteries with obstructed sub-diaphragmatic totally anomalous pulmonary venous connection: a rare case treated with anatomical repair.

作者信息

Meliota Giovanni, Scalzo Gabriele, Vairo Ugo

机构信息

Department of Paediatric Cardiology, Giovanni XXIII Paediatric Hospital, Bari, Italy.

出版信息

Cardiol Young. 2019 Dec;29(12):1536-1538. doi: 10.1017/S1047951119002415. Epub 2019 Oct 30.

DOI:10.1017/S1047951119002415
PMID:31663489
Abstract

Transposition of the great arteries combined with totally anomalous pulmonary venous connection is extremely rare outside of heterotaxy syndrome. Most reported cases have been treated by a modified atrial switch operation. We report the successful treatment of a neonate with this rare association, repaired by arterial switch operation and connection of the pulmonary venous return to the left atrium.

摘要

除了异向性综合征外，大动脉转位合并完全性肺静脉异位连接极为罕见。大多数报道的病例采用改良心房调转术治疗。我们报告了1例患有这种罕见联合病症的新生儿的成功治疗案例，采用动脉调转术及将肺静脉回流连接至左心房进行修复。

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