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[永存共同动脉干(I型)及主动脉弓中断(B型)(作者译)]

[Persistent truncus arteriosus communis (type I) and interruption of the aortic arch (type B) (author's transl)].

作者信息

Hentrich F, Stoermer J

出版信息

Z Kardiol. 1977 Oct;66(10):583-6.

PMID:919669
Abstract

Description of the history, the clinical findings, and the autoptic results in a 5-days-old newborn child with a truncus arteriosus (Type I) and an interrupted aortic arch (Type B). Perfusion of the distal aortic arch by a wide open Ductus arteriosus. Additional anomalies: Atrial septal defect with partial anomalous pulmonary venous drainage of the right lung into the right atrium. Persistant left superior vena cava which leads to the left atrium. Hypoplasia and dysplasia of the left kidney. A tear caused by friction in the left sensorium with intra-and subdural bleeding. Discussion of the clinical, electrocardiographic, radiologic, angiocardiographic and pathologic-anatomical peculiarities of the persistent Truncus arteriosus and of the interrupted aortic arch connected with both defects.

摘要

一名5日龄患有I型共同动脉干和B型主动脉弓中断的新生儿的病史、临床检查结果及尸检结果描述。粗大开放的动脉导管为主动脉弓远端供血。其他异常情况:房间隔缺损,右肺部分肺静脉异常引流至右心房。永存左上腔静脉,引流至左心房。左肾发育不全及发育异常。左侧感觉区因摩擦导致撕裂伴硬膜内和硬膜下出血。讨论了共同动脉干持续存在及与两种缺陷相关的主动脉弓中断的临床、心电图、放射学、心血管造影及病理解剖学特点。

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