法洛四联症合并肺动脉闭锁的先天性心脏病1例并文献复习  

A case of congenital heart disease with Tetralogy of Fallot combined with pulmonary atresia and literature analysis

作　　者：邹明锐 董圣军[1] 刘宝辉[1] 王玉玖[1] Zou Mingrui;Dong Shengjun;Liu Baohui;Wang Yujiu(Cardiovascular Surgery Department,Binzhou Medical University Hospital,Binzhou 256603,China)

机构地区：[1]滨州医学院附属医院(滨州医学院第一临床医学院)心脏大血管外科,滨州256603

出　　处：《国际医药卫生导报》2024年第12期2053-2055,共3页International Medicine and Health Guidance News

基　　金：山东省自然科学基金(ZR2020QH017)。

摘　　要：法洛四联症(TOF)是最常见的紫绀型先天性心脏病,肺动脉闭锁(PA)也是一种较为复杂的先天性心脏畸形。本文对滨州医学院附属医院收治的1例TOF合并PA的先天性心脏病进行报道,手术方案采用外科生物补片进行肺动脉瓣的重建,缝至右心室切口到原肺动脉瓣处以抗肺动脉瓣反流,最后总结TOF/PA的临床表现、影像诊断、手术方案及未来的治疗前景等。Tetralogy of Fallot(TOF)is the most prevalent cyanotic congenital heart disease,and pulmonary atresia(PA)is a relatively complex congenital heart malformation.This paper presented a case of TOF combined with PA admitted to Binzhou Medical University Hospital,where surgical biological mesh was utilized to reconstruct the pulmonary valve and sewed into the original pulmonary valve to prevent pulmonary regurgitation in the right ventricular incision.Finally,this paper summarized the clinical manifestations,imaging diagnosis,surgical plans,and treatment prospect associated with TOF/PA.

关 键 词：法洛四联症 肺动脉闭锁 肺动脉瓣重建 手术方案 

分 类 号：R654.2[医药卫生—外科学]