Abe T, Komatsu S, Chiba M, Asai Y
J Cardiovasc Surg (Torino). 1982 Jan-Feb;23(1):1-5.
Surgical correction was carried out successfully in a severely cyanotic 3-year-old boy with Taussig-Bing malformation. The cardiac anomaly was associated with semilunar valves side by side, and at the same height, a bilateral conus without pulmonary-mitral continuity and subpulmonary ventricular septal defect, on which pulmonary valve overode. The surgical correction consisted of the closure of the VSD by a right atrial approach and modified Senning procedure under profound hypothermic cardiac arrest with surface cooling and limited cardiopulmonary bypass. The patient survived operation and was doing well 10 months after surgery. To our knowledge, no other identical case with Taussig-Bing malformation has been corrected successfully by this procedure nor has previously been reported.
一名患有陶西格-宾畸形的3岁重度青紫男孩成功接受了手术矫正。心脏异常表现为半月瓣并列且处于同一高度，双侧圆锥无肺-二尖瓣连续性，并有肺动脉瓣下室间隔缺损，肺动脉瓣骑跨于该缺损之上。手术矫正包括在深度低温心脏停搏及体表降温、有限体外循环下，经右心房入路闭合室间隔缺损并施行改良森宁手术。患者术后存活，术后10个月情况良好。据我们所知，此前尚无其他相同的陶西格-宾畸形病例通过该手术成功矫正，也未有相关报道。
