Yoshida M, Yagihara T, Uemura H, Yamashita K, Kawahira Y, Yoshizumi K
Department of Cardiovascular Surgery, National Cardiovascular Center, Osaka, Japan.
Jpn J Thorac Cardiovasc Surg. 1998 Nov;46(11):1177-81. doi: 10.1007/BF03217897.
We describe herein a successful biventricular repair in a 21-year-old male who had severe hypoplasia of isomeric right appendages. He had previously undergone the conventional Glenn procedure at the age of one and a half years. Although he had grown uneventfully until adolescence, cyanosis as well as fatigue than gradually became worse. When referred to us for further treatment, we deemed a Fontan type procedure to be contraindicated, because of the hypoplastic nature of the right pulmonary artery, and the presence of abundant collateral arteries supplying the right lung. In terms of ventricular morphology, however, because both apical components were present, separated by the hypoplastic septum, biventricular repair seemed feasible. Initially, the Glenn anastomosis was taken down, and systemic-to-pulmonary shunts were constructed via a median sternotomy to both the right and left pulmonary arteries. This was followed by surgical division of the developed collaterals to the right lung via the right thoracotomy. Definitive biventricular repair was then carried out by reconstructing the pulmonary arteries and right ventricular outflow tact, separating and rerouting within the ventricles using a EPTFE patch, and achieving redirection of blood within the atriums using bovine pericardium. Such staged surgical approaches, although extensive, can provide useful options when seeking definitive repair in grown-up patients with complicated malformations.
我们在此描述了一例对一名患有右心耳异构严重发育不全的21岁男性患者成功实施的双心室修复手术。他在一岁半时曾接受过传统的格林手术。尽管他在青春期前生长过程顺利,但紫绀和疲劳症状逐渐加重。当他前来我们这里寻求进一步治疗时,由于右肺动脉发育不全以及存在大量供应右肺的侧支动脉,我们认为Fontan类手术是禁忌的。然而,就心室形态而言,由于两个心尖部分均存在,被发育不全的室间隔分隔开,双心室修复似乎是可行的。最初,拆除格林吻合口,并通过正中胸骨切开术在左右肺动脉上构建体肺分流。随后,通过右胸切开术对发育的右肺侧支进行手术切断。然后通过重建肺动脉和右心室流出道、使用聚四氟乙烯补片在心室内进行分隔和改道,以及使用牛心包实现心房内血液改道,进行最终的双心室修复。这种分期手术方法虽然复杂,但在为患有复杂畸形的成年患者寻求最终修复时可提供有用的选择。