Thiene G, Gallucci V, Macartney F J, Del Torso S, Pellegrino P A, Anderson R H
Circulation. 1979 Jan;59(1):173-8. doi: 10.1161/01.cir.59.1.173.
The anatomy of 58 specimens of aortic outflow tract atresia was studied. All cases had situs solitus and levocardia, 37 had atrioventricular (AV) concordance, two had common inlet to a right ventricle and 19 had mitral atresia. The great arteries were normally interrelated in all cases. Fifty-one cases had an intact ventricular septum, while seven presented with a ventricular septal defect (VSD). Of the seven with VSD, in two it was associated with a common AV orifice draining exclusively into the right ventricle in the presence of a rudimentary left ventricular chamber. In one case a small VSD accompanied combined mitral and aortic atresia. In the other four cases the left ventricles and mitral valves were fairly normal in size; the VSD was subpulmonary in three cases, due to infundibuloventricular malalignment, and perimembranous in one. These last four cases are of particular interest since they could be amenable to surgical correction. Possible approaches to surgical treatment and morphologic features pertinent to them are described and discussed.
对58例主动脉流出道闭锁标本的解剖结构进行了研究。所有病例均为右位心且心脏左位,37例房室一致,2例右心室有共同入口,19例二尖瓣闭锁。所有病例中,大动脉关系正常。51例室间隔完整,7例存在室间隔缺损(VSD)。在7例有室间隔缺损的病例中,2例与共同房室口相关,该房室口仅引流至存在发育不全左心室腔的右心室。1例病例中,小室间隔缺损合并二尖瓣和主动脉闭锁。在其他4例病例中,左心室和二尖瓣大小基本正常;3例室间隔缺损位于肺动脉瓣下,系漏斗部与心室排列不齐所致,1例为膜周部室间隔缺损。最后这4例病例特别值得关注,因为它们可能适合手术矫正。文中描述并讨论了可能的手术治疗方法及其相关的形态学特征。