室间隔缺损的形态学。

Perspectives in pediatric pathology Pub Date : 1984-01-01
R H Anderson, C C Lenox, J R Zuberbuhler
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引用次数: 0

摘要

室间隔缺损(Ventricular septal缺损,VSD)是最常见的先天性心脏病变,既可单独发生,也可在含有更复杂病变的心脏中发生。通常,缺陷位于两个心室之间,每个心室都连接到一个单独的心房和一个单独的大动脉,如果忽略任何相关病变的影响,手术或自发关闭室间隔基本上可以纠正循环。在其他情况下,室间隔是循环的一个组成部分,或者是因为心房只连接到一个心室,或者因为心室只产生一个通畅的大动脉,或者两个大动脉都来自同一个心室。在这种情况下,血液循环依赖于vsd,如果不使用导管或类似装置旁路,则无法通过手术关闭缺损。在所有这些情况下,VSD采用三种基本形式之一。通常,VSD直接靠近由心脏瓣膜连接环形成的心脏纤维骨架。室间隔的膜性部分是这个骨架的一个组成部分,这些缺陷被称为膜周。这些缺损并不总是占据鼻中隔的同一部分。它们可以主要延伸到肌隔的入口、小梁或出口部分,或者是合流延伸到两个或所有这些部分。不太常见的是,室间隔缺损可能只存在于肌肉隔膜内。这种肌肉缺陷也可局限于鼻中隔的入口、小梁或出口部分。它们可以是多个或与其他类型之一共存。第三种也是最不常见的类型是室间隔,由于没有外隔膜,它被主动脉瓣和肺动脉瓣的连接环所覆盖。这种缺陷可能有肌肉的后下缘,也可能延伸到膜周。鉴别一个缺陷是膜周性的还是肌肉性的,以及它相对于肌肉间隔不同部分的位置,同时提供了有关传导轴与缺陷的关系以及其自发闭合的机会的信息。
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The morphology of ventricular septal defects.

Ventricular septal defect (VSD) is the most common congenital cardiac lesion, occurring either in isolation or in hearts containing more complex lesions. Usually, the defect is between two ventricles, each of which is connected to a separate atrium and to a separate great artery, and surgical or spontaneous closure of the VSD basically corrects the circulation if the effects of any associated lesion are ignored. In other situations, the VSD is an integral part of the circulation, either because the atria connect to only one ventricle or because the ventricles give rise to only one patent great artery or else both great arteries arise from the same ventricle. When in such circumstances the circulation is VSD-dependent and the defect cannot be surgically closed without bypassing it with a conduit or similar device. In all of these situations, the VSD takes one of three basic forms. Usually, the VSD abuts directly upon the fibrous skeleton of the heart formed by the conjoined rings of the cardiac valves. The membranous part of the ventricular septum is an integral part of this skeleton, and these defects are termed perimembranous. These defects do not always occupy the same part of the septum. They may extend mostly into either the inlet, trabecular, or outlet parts of the muscular septum, or else be confluent extending into two or all these parts. Less commonly, VSD may be exclusively contained within the muscular septum. Such muscular defects can also be confined to either the inlet, trabecular, or outlet parts of the septum. They may be multiple or coexist with one of the other types. The third and least common type is a VSD which is roofed by the conjoined rings of the aortic and pulmonary valves because of absence of the outer septum. Such a defect may have a muscular posteroinferior rim or may extend to become perimembranous. Identifying a defect as perimembranous or muscular, together with its location relative to the different parts of the muscular septum, gives at the same time information concerning the site of the conduction axis in relation to the defect and its chances of spontaneous closure.

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