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室间隔缺损合并肺动脉闭锁的产前诊断

Prenatal diagnosis of pulmonary atresia with ventricular septal defect.

作者信息

Yang Shui-Hua, Luo Peng-Hui, Tian Xiao-Xian, Li Xin-Yan, Li Xue-Qin, Yang Zuo-Jian, Li Sheng-Li

机构信息

Department of Ultrasound, The Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.

Department of Oncology, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

J Med Ultrason (2001). 2018 Apr;45(2):341-344. doi: 10.1007/s10396-017-0809-2. Epub 2017 Jul 27.

Abstract

Pulmonary atresia with ventricular septal defect (PA-VSD) is a rare complex congenital heart defect. Major artery-pulmonary collateral arteries (MAPCAs) are characteristic of PA-VSD. Prenatal diagnosis can be achieved in most cases of PA-VSD with recent advances in echocardiography. However, it is extremely rare that all MAPCAs can be observed on the echocardiograph. Here, we report a case of prenatally diagnosed type C PA-VSD in which all the MAPCAs could be seen on the echocardiograph, with the diagnosis supported by autopsy evidence.

摘要

肺动脉闭锁合并室间隔缺损(PA-VSD)是一种罕见的复杂先天性心脏缺陷。体-肺侧支动脉(MAPCAs)是PA-VSD的特征。随着超声心动图技术的最新进展,大多数PA-VSD病例在产前即可得到诊断。然而,在超声心动图上能够观察到所有的MAPCAs极为罕见。在此,我们报告一例产前诊断为C型PA-VSD的病例,该病例在超声心动图上可观察到所有的MAPCAs,且尸检证据支持该诊断。

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