Burke R P, Rosenfeld H M
Department of Cardiology, Children's Hospital, Boston, MA 02115.
Ann Thorac Surg. 1994 Aug;58(2):543-5. doi: 10.1016/0003-4975(94)92250-0.
Aortopulmonary septal defect, interruption of the aortic arch, and anomalous origin of the right pulmonary artery from the aorta comprised a challenging constellation of defects in a 13-day-old neonate, who underwent complete repair without homograft tissue or synthetic graft. After the aorta was separated from the pulmonary artery, the descending aorta was anastomosed to the septal defect in the ascending aorta. The right pulmonary artery was anastomosed to the septal defect in the main pulmonary artery, anterior to the aorta. The postoperative course was uncomplicated, and the potential for growth of both great vessels was optimized.
主动脉肺动脉间隔缺损、主动脉弓中断以及右肺动脉起源于主动脉异常,这些构成了一名13日龄新生儿的一组具有挑战性的复杂缺损,该患儿在未使用同种异体移植组织或合成移植物的情况下接受了完全修复。在主动脉与肺动脉分离后,降主动脉与升主动脉的间隔缺损处进行了吻合。右肺动脉在主动脉前方与主肺动脉的间隔缺损处进行了吻合。术后过程顺利,两根大血管的生长潜力得到了优化。