Flórez M, Attie F, Muñoz-Castellanos L, Vargas Barrón J, Ovseyevitz J, Buendía A, Zavaleta D
Arch Inst Cardiol Mex. 1986 Jan-Feb;56(1):63-9.
Twenty-five cases of double-inlet left ventricle, 23 in atrial situs solitus and 2 with dextroisomerism are described. Twenty had both atrioventricular valves and in 3 a common atrioventricular valve connected to the left ventricle. In rest, the left atrioventricular valve was straddling over the left-sided right ventricle in about 15%. The position of the rudimentary right ventricle varied from superior, anterior and to the right of left ventricle (6 with transposition and 9 with concordant ventriculo arterial connection), to superior anterior and to the left of left ventricle (10 cases, all with transposition). Five cases had stenosis of the left atrioventricular valve and 2 stenosis of the right one. In 11, the clinical presentation was dominated by cyanosis, reduced pulmonary blood flow and right to left shunt. The rest had cyanosis and congestive heart failure. Five patients with right ventricle on the left had complete atrioventricular block, 9 right AQRS orientation and all of them findings of left ventricle hypertrophy. Three cases showed initial Q wave in VI and one left bundle branch block. Cases with right ventricle on the right, had left QRS orientation, left ventricle hypertrophy and 2 complete atrioventricular block. Cross-sectional echoes showed in 13, two atrioventricular valves committed to the left ventricle; in 3 of them the right ventricle was visualized. In 22 cases angiography determined the type of atrioventricular connection. Double inlet left ventricle is one of the most challenging diagnosis in congenital heart disease. Considering its lack of clinical specificity and according to our results, the electrocardiogram, echocardiogram and angiographic findings are of great help for its identification.
本文描述了25例双入口左心室病例,其中23例心房正位,2例心房异构。20例有两个房室瓣,3例有连接到左心室的共同房室瓣。其余病例中,约15%的左房室瓣跨越左侧右心室。残存右心室的位置变化多样,从左心室的上方、前方和右侧(6例为转位,9例为心室-动脉连接一致)到左心室的上方、前方和左侧(10例,均为转位)。5例有左房室瓣狭窄,2例有右房室瓣狭窄。11例的临床表现以发绀、肺血流量减少和右向左分流为主。其余病例有发绀和充血性心力衰竭。5例左位右心室患者有完全性房室传导阻滞,9例右心室QRS波群电轴向右,所有患者均有左心室肥厚表现。3例在V1导联出现初始Q波,1例有左束支传导阻滞。右位右心室的病例有左心室QRS波群电轴、左心室肥厚,2例有完全性房室传导阻滞。13例经胸超声心动图显示两个房室瓣均连于左心室;其中3例可显示右心室。22例经心血管造影确定了房室连接类型。双入口左心室是先天性心脏病中最具挑战性的诊断之一。鉴于其缺乏临床特异性,根据我们的研究结果,心电图、超声心动图和血管造影检查结果对其诊断有很大帮助。