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患有肺动脉闭锁和室间隔缺损的婴儿的罕见血管环。

Unusual vascular ring in infant with pulmonary atresia and ventricular septal defect.

作者信息

McKay R, Stark J, de Leval M

出版信息

Br Heart J. 1982 Aug;48(2):180-3. doi: 10.1136/hrt.48.2.180.

Abstract

A 3-day-old infant investigated for cyanotic heart disease was found to have partial DiGeorge syndrome and pulmonary atresia with ventricular septal defect. The only source of pulmonary blood flow was a right-sided persistent ductus arteriosus which originated from an aberrant right subclavian artery. Such a vascular ring has not been described previously. Surgical treatment included a left-sided prosthetic shunt in infancy followed by resection of the ligamentum arteriosum and right subclavian artery during the second year of life.

摘要

一名因患青紫型心脏病接受检查的3日龄婴儿,被发现患有部分迪格奥尔格综合征以及伴有室间隔缺损的肺动脉闭锁。肺血流的唯一来源是一条起源于迷走右锁骨下动脉的右侧动脉导管未闭。此前尚未有过这种血管环的描述。手术治疗包括在婴儿期进行左侧人工分流,然后在患儿1岁时切除动脉韧带和右锁骨下动脉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01b/481224/b236ce715861/brheartj00152-0085-a.jpg

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