Moene R J, Oppenheimer-Dekker A, Bartelings M M
Am J Cardiol. 1983 Jun;51(10):1701-4. doi: 10.1016/0002-9149(83)90213-8.
In 126 hearts with transposition of the great arteries (TGA), morphologic features of the right ventricular (RV) outflow tract were analyzed. Distinct anatomic outflow tract obstruction was found in 15 of the 55 hearts with a ventricular septal defect (VSD) (27%): 12 had a perimembranous defect (predominantly extending into the infundibulum), 2 had an inlet, and 1 had an infundibular defect. In 12 hearts, outflow tract obstruction was caused by anterior displacement of infundibular septum and ventriculoinfundibular fold; in 3 hearts, it was caused by bulging of the trabecula septomarginalis or ventriculoinfundibular fold, or both. Of 71 hearts with an intact ventricular septum, only 2 (3%) had RV outflow tract obstruction: 1 had a trabecula in front of the aortic ostium and in the other an aberrant hypertrophic muscle bundle crossed the RV cavity, obstructing the entrance to the infundibulum. Associated malformations included aortic arch malformations (6 cases) and tricuspid valve anomalies (6 cases). Thus, anatomic RV outflow tract obstruction may constitute a complicating factor in TGA, notably in cases with VSD. A systemic RV blood pressure may trigger hypertrophy, resulting in progression of the obstruction; establishing normal RV pressure by a "switch" procedure might prevent this progression.
在126例大动脉转位(TGA)患者的心脏中,对右心室(RV)流出道的形态特征进行了分析。在55例伴有室间隔缺损(VSD)的心脏中,有15例(27%)发现明显的解剖性流出道梗阻:12例为膜周部缺损(主要延伸至漏斗部),2例为流入道缺损,1例为漏斗部缺损。在12例心脏中,流出道梗阻是由漏斗间隔和室漏斗皱襞向前移位引起的;在3例心脏中,是由隔缘肉柱或室漏斗皱襞膨出或两者共同引起的。在71例室间隔完整的心脏中,只有2例(3%)存在RV流出道梗阻:1例在主动脉口前方有一条小梁,另1例有一条异常肥厚的肌束穿过RV腔,阻塞了漏斗部入口。相关畸形包括主动脉弓畸形(6例)和三尖瓣异常(6例)。因此,解剖性RV流出道梗阻可能是TGA的一个并发症因素,尤其是在伴有VSD的病例中。体循环RV血压可能引发肥厚,导致梗阻进展;通过“调转”手术建立正常的RV压力可能会阻止这种进展。