De Tommasi S M, Borghi A, Carminati M, Valsecchi O, Velitti F, Troiani P, Valsecchi M G, Zonca A
G Ital Cardiol. 1984 Jun;14(6):424-30.
We describe six patients with situs solitus of viscera and atria, dextrocardia, atrioventricular discordance, ventricular septal defect, double outlet from the morphological right ventricle, pulmonic stenosis and levomalposition of the aorta. Four patients were male and two female; their age ranged from 3.5 to 31 years (mean 13.8 years). All had various degrees of disability, and presented with cyanosis, clubbing and high hematocrit levels. One patient had an atrio-ventricular block that varied from first to third degree; another patient showed intermittent junctional rhythm. At angiography the ventricular septum appeared to be almost perpendicular to the frontal plane in most cases, so that the anteroposterior projection resulted in a true axial view. One overriding left atrioventricular valve and one straddling right atrio-ventricular valve were demonstrated; no significant incompetence of either valve was observed. The ventricular septal defect was always single and related to the subpulmonary outflow. Pulmonic stenosis was valvular in every patient; an additional infundibular obstruction was present in one case. In two cases an additional stenosis was discovered at the supravalvular level. The left pulmonary branch was stenotic in one case; it was hypoplastic, with controlateral dilatation, in two cases; both pulmonary arteries were dilated in one case. The aorta was always to the left of the pulmonary artery, either anterior or side by side. Three patients were operated on in different Institutions: one had a pulmonic valvotomy at the age of six years; one, aged twenty, had a right Blalock-Taussig shunt; the third, with overriding left atrioventricular valve, underwent a modified Fontan operation at the age of thirty years with success.(ABSTRACT TRUNCATED AT 250 WORDS)
我们描述了6例具有内脏和心房正位、右位心、房室不一致、室间隔缺损、形态学右心室双出口、肺动脉狭窄及主动脉左旋位的患者。4例为男性,2例为女性;年龄范围为3.5至31岁(平均13.8岁)。所有患者均有不同程度的残疾,表现为发绀、杵状指和高血细胞比容水平。1例患者存在一度至三度不等的房室传导阻滞;另1例患者表现为间歇性交界性心律。血管造影显示,多数情况下室间隔几乎与额面垂直,因此前后位投影可获得真正的轴位视图。发现1例左侧房室瓣骑跨和1例右侧房室瓣跨立;未观察到任何一个瓣膜有明显关闭不全。室间隔缺损均为单一型,与肺动脉下流出道相关。每位患者的肺动脉狭窄均为瓣膜型;1例还存在漏斗部梗阻。2例在瓣膜上水平发现额外狭窄。1例左肺动脉分支狭窄;2例发育不全,对侧扩张;1例双侧肺动脉均扩张。主动脉总是位于肺动脉左侧,或在前或并列。3例患者在不同机构接受了手术:1例6岁时接受了肺动脉瓣切开术;1例20岁时进行了右布莱洛克-陶西格分流术;第3例有左侧房室瓣骑跨,30岁时接受了改良Fontan手术,手术成功。(摘要截短于250字)