Malec E, Mroczek T, Pajak J, Kordon Z
Department of Pediatric Cardiac Surgery, Polish-American Children's Hospital, Collegium Medicum, Jagiellonian University, Kraków.
Ann Thorac Surg. 2000 Jan;69(1):278-80. doi: 10.1016/s0003-4975(99)01261-8.
The coexistence of tricuspid atresia and common arterial trunk is extremely rare. We present a successful three-stage surgical treatment of this defect. The first stage included disconnection of the pulmonary arteries from the common trunk, atrial septectomy and systemic-to-pulmonary shunt; the second stage, a hemi-Fontan procedure; and the third stage, a fenestrated Fontan completion. The child is now 8 years old and is developing well.
三尖瓣闭锁与共同动脉干并存极为罕见。我们介绍了对此缺陷成功进行的三阶段手术治疗。第一阶段包括将肺动脉与共同动脉干离断、房间隔切除术及体肺分流术；第二阶段，进行半Fontan手术；第三阶段，完成开窗Fontan手术。患儿现8岁，发育良好。
