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先天性矫正型大动脉转位:32例形态学研究

Congenitally corrected transposition of the great arteries: morphologic study of 32 cases.

作者信息

Allwork S P, Bentall H H, Becker A E, Cameron H, Gerlis L M, Wilkinson J L, Anderson R H

出版信息

Am J Cardiol. 1976 Dec;38(7):910-23. doi: 10.1016/0002-9149(76)90804-3.

Abstract

The detailed anatomy of the heart is described in 32 autopsy cases of congenitally corrected transposition of the great arteries.Tis condition is defined as the combination of atrioventricular (A-V) discordance and transposition of the great arteries. Examples of primitive (single) ventricle with "inverted" (that is, left-sided in situs solitus) outlet chamber are excluded. Six hearts with A-V discordance and pulmonary atresia are described in an appendix. In 29 cases of corrected transposition the heart was in situs solitus; in 3 it was in situs inversus totalis. Only 5 of these 32 hearts had no potential for intracardiac shunting. Anomalies of the tricuspid valve (91 percent of cases), ventricular septal defect (78 percent) and pulmonary outflow tract obstruction (44 percent) occurred with sufficient frequency to be considered part of the basic malformation and are described in detail. The precise anatomy and disposition of the A-V valve tension apparatus, the coronary arteries and the conducting tissues are described with special reference to possible surgical approaches for repair of the anomalies. In two hearts with situs solitus the aortic valve was right-sided with respect to the pulmonary valve. This finding is important for both diagnosis and nomenclature.

摘要

在32例先天性矫正型大动脉转位的尸检病例中描述了心脏的详细解剖结构。这种情况被定义为房室(A-V)不一致和大动脉转位的组合。排除了具有“倒置”(即,在正常位置中位于左侧)流出腔的原始(单)心室的例子。附录中描述了6例伴有A-V不一致和肺动脉闭锁的心脏。在29例矫正型转位病例中,心脏处于正常位置;在3例中,心脏处于完全反位。这32颗心脏中只有5颗没有心内分流的可能性。三尖瓣异常(91%的病例)、室间隔缺损(78%)和肺流出道梗阻(44%)出现的频率足以被视为基本畸形的一部分,并进行了详细描述。特别参考了修复这些异常的可能手术方法,描述了A-V瓣膜张力装置、冠状动脉和传导组织的精确解剖结构和位置。在两例心脏处于正常位置的病例中,主动脉瓣相对于肺动脉瓣位于右侧。这一发现对诊断和命名都很重要。

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