Riggs Kyle W, Price Nina M, Szugye Nicholas, Goldstein Bryan H, Morales David L S
Cincinnati Children's Hospital Medical Center, Heart Institute, Cincinnati, OH, USA.
Ann Pediatr Cardiol. 2019 Sep-Dec;12(3):318-320. doi: 10.4103/apc.APC_152_18.
We report a case of hypoplastic left heart syndrome with an anomalous left coronary artery from the pulmonary artery (ALCAPA) identified intraoperatively during the Stage-II palliation. Due to recurring ventricular fibrillation on sternotomy, a hybrid Stage-I palliation was performed. During comprehensive Stage-II, the ALCAPA was reimplanted in the neoaorta and measures, including a nontraditional Damus connection/arch reconstruction and classic bilateral Glenn procedures, were taken to avoid compression of the coronary artery. After a successful Fontan procedure, he continues to do well at 5 years old, becoming the first patient reported in the literature to survive all the three stages of single-ventricle palliation.
我们报告了一例左心发育不全综合征病例,该病例在二期姑息治疗术中发现存在源自肺动脉的异常左冠状动脉(ALCAPA)。由于胸骨切开时反复出现心室颤动,遂进行了一期杂交姑息治疗。在全面的二期治疗中,将ALCAPA重新植入新主动脉,并采取了包括非传统Damus连接/主动脉弓重建和经典双侧格林手术在内的措施,以避免冠状动脉受压。在成功完成Fontan手术之后,他在5岁时情况持续良好,成为文献报道中首例成功度过单心室姑息治疗所有三个阶段的患者。