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先天性心脏病伴发的先天性心外畸形

Congenital extracardial malformations accompanying congenital heart disease.

作者信息

Gallo P, Nardi F, Marinozzi V

出版信息

G Ital Cardiol. 1976;6(3):450-9.

PMID:1010196
Abstract

A statistical review of 1,354 autopsies performed in cases of congenital heart disease in three major Italian hospitals was carried out. In 446 cases one or more extracardial malformations were found; those most commonly encountered were malformations of the urinary tract, anomalies of the respiratory tract, malformations of the intestine and spleen and trisomy 21. Ventricular septal defects and persistent common atrioventricular canals occurred in a higher percentage of cases with extracardial malformations than in those where congenital heart defects were the only malformations. The reverse was true of endocardial fibroelastosis and transposition of the great vessels. Ventricular septal defects are particularly common in the Klippel-Feil syndrome, in trisomy 18 and, together with a persistent common atrioventricular canal and atrial septal defects, in trisomy 21. The typical picture of so-called "congenital heart disease associated with asplenia" was found in cases with splenic agenesis, either with or without situs inversus viscerum, but also in cases with situs inversus viscerum without asplenia.

摘要

对意大利三家主要医院进行的1354例先天性心脏病尸检进行了统计回顾。在446例病例中发现了一种或多种心外畸形;最常见的是泌尿系统畸形、呼吸道异常、肠道和脾脏畸形以及21三体综合征。室间隔缺损和持续性共同房室通道在有心外畸形的病例中出现的比例高于仅患有先天性心脏缺陷的病例。心内膜弹力纤维增生症和大动脉转位则相反。室间隔缺损在Klippel-Feil综合征、18三体综合征中尤为常见,在21三体综合征中与持续性共同房室通道和房间隔缺损一起也很常见。在无脾症病例中,无论是否伴有内脏反位,都发现了所谓“与无脾症相关的先天性心脏病”的典型表现,但在无无脾症的内脏反位病例中也有发现。

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