Van Den Bogaert-Van Heesvelde A M, Derom F, Kunnen M, Van Egmond H, Devloo-Blancquaert A
J Thorac Cardiovasc Surg. 1978 Aug;76(2):195-7.
A superior vena cava-right pulmonary artery (SVC-RPA) anastomosis was constructed in a 2-year-old boy with tetralogy of Fallot. Ten years later and 5 years after "corrective" surgery without removal of the shunt, cyanosis and heart failure developed. Stereocineangiography and lung scanning revealed arteriovenous fistulas and dilated vessels in the right lung. The SVC-RPA anastomosis was taken down, the SVC being reimplanted in the right atrium and the RPA end being closed with a few stitches. Neither lobectomy nor pneumonectomy was performed. Immediately after the operation and during a follow-up period of almost 2 years, the boy has remained asymptomatic. Whenever a correction is planned in a patient with SVC-RPA anastomosis, the vessels of the right lung should be examined by scanning and angiography. If important arteriovenous fistulas do exist, the affected lung should be excluded from the pulmonary artery circulation.
为一名患有法洛四联症的2岁男孩构建了上腔静脉-右肺动脉(SVC-RPA)吻合术。10年后,在未拆除分流器的“矫正”手术后5年,出现了紫绀和心力衰竭。立体心血管造影和肺部扫描显示右肺存在动静脉瘘和血管扩张。拆除了SVC-RPA吻合术,将上腔静脉重新植入右心房,右肺动脉端用几针缝合关闭。未进行肺叶切除术或全肺切除术。术后立即及近2年的随访期间,该男孩一直无症状。每当计划对患有SVC-RPA吻合术的患者进行矫正时,应通过扫描和血管造影检查右肺血管。如果确实存在重要的动静脉瘘,应将受影响的肺排除在肺动脉循环之外。