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罕见的共同动脉干伴右肺动脉闭锁和体肺侧支血管形成。

Unusual Case of Common Arterial Trunk With Atresia of the Right Pulmonary Artery and Aortopulmonary Collaterals.

机构信息

Department of Cardiovascular and Thoracic Surgery, University of Louisville School of Medicine, Norton Children's Hospital, Louisville, KY, USA.

Department of Radiology, Norton Children's Hospital, Louisville, KY, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2020 Jul;11(4):534-536. doi: 10.1177/2150135120913807.

DOI:10.1177/2150135120913807
PMID:32645783
Abstract

We describe a two-year-old African girl with late diagnosis of unusual case of common arterial trunk with two separate pulmonary artery branch origins from the ascending aorta, hypoplastic right pulmonary artery that becomes atretic and reconstitutes at hilum, and three aortopulmonary collaterals providing right lung blood supply. She underwent single-stage intracardiac repair and unifocalization of collaterals.

摘要

我们描述了一例罕见的共同动脉干病例,一名两岁的非洲女孩就诊时已较晚,该病源于升主动脉的两个独立的肺动脉分支,右肺动脉发育不良且在肺门处成为闭锁,有三条体肺侧支为右肺提供血液供应。她接受了一期心内修复和侧支的单灶化治疗。

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