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先天性矫正型大动脉转位合并房室间隔缺损

Congenitally corrected transposition with atrioventricular septal defect.

作者信息

Attie F, Iturralde P, Zabal C, Rijlaarsdam M, Buendia A, Colin L, Vargas-Barron J, Muñoz-Castellanos L

机构信息

Instituto Nacional de Cardiologia Ignacio Chavez, Mexico DF, Mexico.

出版信息

Cardiol Young. 1998 Oct;8(4):472-8. doi: 10.1017/s1047951100007137.

Abstract

We describe 4 cases of congenitally corrected transposition associated with atrioventricular septal defect, diagnosed by echocardiography and angiocardiography. Two had usual atrial arrangement and two had mirror imaged atrial arrangement . All cases were associated with subpulmonary valvar stenosis. All patients presented with cyanosis and were in sinus rhythm. Atrioventricular septal defect with common atrioventricular junction was easily diagnosed on the basis of a common atrioventricular valve permitting interatrial and interventricular communications. All patients had balanced right and left ventricles. The echocardiographic recognition of the ventricles was based on the presence of the moderator band within the morphologically right ventricle, the characteristics of the apical septal trabeculations, and the shape of the ventricles. Angiocardiographic recognition of the ventricles was achieved on the basis of right and left ventriculography. In one case with usual atrial arrangement, we recorded two His bundle potentials, one anteriorly and another posteriorly. Atrial stimulation revealed blocked atrioventricular conduction at the level of the posterior bundle, and normal atrioventricular conduction through the anterior bundle. In both cases with atrial mirror-imagery, only a posterior His bundle potential was found, with normal atrioventricular conduction revealed by atrial stimulation The clinical course with this combination depends on the other lesions present in addition to the common atrioventricular valve. Our electrophysiological studies show that the conduction system in presence of a common atrioventricular valve is as expected for congenitally corrected transposition with two atrioventricular valves.

摘要

我们描述了4例与房室间隔缺损相关的先天性矫正型大动脉转位病例,这些病例通过超声心动图和心血管造影诊断。其中2例心房排列正常,2例心房呈镜像排列。所有病例均伴有肺动脉瓣下狭窄。所有患者均有发绀,且为窦性心律。基于允许心房和心室间交通的共同房室瓣,伴有共同房室连接的房室间隔缺损很容易诊断。所有患者的左右心室均平衡。超声心动图对心室的识别基于形态学上的右心室内存在节制索、心尖间隔小梁的特征以及心室的形状。心血管造影对心室的识别是基于左右心室造影。在1例心房排列正常的病例中,我们记录到两个希氏束电位,一个在前,另一个在后。心房刺激显示后束水平存在房室传导阻滞,而通过前束的房室传导正常。在两例心房镜像排列的病例中,仅发现一个后希氏束电位,心房刺激显示房室传导正常。这种组合的临床病程取决于除共同房室瓣外还存在的其他病变。我们的电生理研究表明,在存在共同房室瓣的情况下,传导系统与具有两个房室瓣的先天性矫正型大动脉转位预期情况相同。

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