Thiene G, Daliento L, Frescura C, De Tommasi M, Macartney F J, Anderson R H
Br Heart J. 1981 Apr;45(4):393-401. doi: 10.1136/hrt.45.4.393.
Sixty-two hearts without a patent exit from the left atrium to the ventricular mass have been studied. All had situs solitus and laevocardia. The material consisted of 32 cases with coexistent aortic atresia and 30 cases with patent aortic root. Five hearts with aortic atresia were biventricular with atrioventricular concordance and imperforate left atrioventricular valves, and 27 hearts were univentricular of right ventricular type, with absent left atrioventricular connection. The anatomy of this group was uniform, with extreme hypoplasia of all the left cardiac segments. Among the cases with patent aortic root, five were biventricular, with atrioventricular concordance and imperforate left atrioventricular valves, and 24 had absent left atrioventricular connection, 15 with univentricular heart of right ventricular type and nine with univentricular heart of left ventricular type. The final heart had double inlet univentricular of left ventricular type with an imperforate left atrioventricular valve. In this second group the aorta was larger in cases with discordant ventriculoarterial connection or in those with double outlet from the main ventricular chamber. A normal sized aorta without aortic arch obstruction was observed in nine instances. These are of great interest in terms of surgical anatomy since definitive palliation may be feasible.
对62例左心房至心室团无开放通道的心脏进行了研究。所有病例均为正位心和左位心。研究材料包括32例合并主动脉闭锁的病例和30例主动脉根部开放的病例。5例主动脉闭锁的心脏为双心室,房室一致,左房室瓣闭锁;27例为右心室型单心室,左房室连接缺如。该组病例的解剖结构一致,所有左心段均极度发育不全。在主动脉根部开放的病例中,5例为双心室,房室一致,左房室瓣闭锁;24例左房室连接缺如,其中15例为右心室型单心室,9例为左心室型单心室。最后1例为左心室型双入口单心室,左房室瓣闭锁。在第二组中,心室动脉连接不一致或主心室双出口的病例中,主动脉较大。9例观察到主动脉大小正常且无主动脉弓梗阻。就手术解剖而言,这些情况极具意义,因为可能可行确定性姑息治疗。