左冠状动脉起源于主动脉弓异常与左心发育不全综合征相关。

Anomalous Origin of Left Coronary Artery From Aortic Arch Associated With Hypoplastic Left Heart Syndrome.

机构信息

Department of Cardiovascular Surgery, Fukui Cardiovascular Center, Fukui, Japan.

Department of Pediatric Cardiovascular Surgery, Children's Medical Center, Kyoto Prefectural University of Medicine, Kyoto, Japan.

出版信息

Ann Thorac Surg. 2019 Jan;107(1):e51-e53. doi: 10.1016/j.athoracsur.2018.05.028. Epub 2018 Jun 8.

DOI:10.1016/j.athoracsur.2018.05.028

PMID:29890146

Abstract

Anomalous origin of the coronary artery from the aortic arch associated with hypoplastic left heart syndrome is an extremely rare anomaly. Coronary anomalies can significantly deteriorate the clinical outcomes of hypoplastic left heart syndrome. We describe the case of a newborn with concomitant hypoplastic left heart syndrome and abnormal origin of the left coronary artery arising from the distal aortic arch.

摘要

升主动脉弓发出的冠状动脉异常起源合并左心发育不良综合征是一种极其罕见的畸形。冠状动脉异常可显著恶化左心发育不良综合征的临床结局。我们描述了一例新生儿同时患有左心发育不良综合征和左冠状动脉起源于远端升主动脉弓的异常。