Duong Phuoc, Papaioannou Vasileios, Moharam-Elgamal Sarah, Kang Sok-Leng
Department of Pediatric Cardiology, Alder Hey Children's Hospital, Liverpool, UK.
Department of Adult Congenital Heart Disease, Liverpool Heart and Chest Hospital, Liverpool, UK.
Eur Heart J Case Rep. 2022 Oct 3;6(10):ytac382. doi: 10.1093/ehjcr/ytac382. eCollection 2022 Oct.
Persistent left superior vena cava (LSVC) with connection to the left atrium (LA) is a rare anomaly with serious clinical implications. Depending on the direction of flow through the intracardiac shunt, clinical presentation varies from cyanosis or paradoxical embolism to overt right heart failure.
A 26-year-old man with repaired ventricular septal defect (VSD) during infancy presented with symptoms of progressive exercise intolerance. Cardiac imaging revealed a large defect at the posterior wall of the LSVC above its entry to the coronary sinus (CS), connecting the LSVC with the LA and resulting in diversion of pulmonary venous return to the CS. All pulmonary veins connect normally to the LA. The large left-to-right intracardiac shunt led to significant right ventricular dilation and tricuspid regurgitation. He underwent successful anatomical repair with transcatheter implantation of covered stent from LSVC to the CS, redirecting pulmonary venous return to the LA. At 1 year follow up, his exercise capacity had improved, and cardiac imaging showed complete seal of the LSVC defect without obstruction to pulmonary venous return.
Our case is the first to our knowledge to report this unusual anatomic variant of LSVC to LA connection, and complete repair by transcatheter treatment. Previous case reports of other forms of LSVC to LA connection were treated with surgery or device occlusion without reconnection of LSVC. This case highlights the efficacy and safety of innovative percutaneous techniques in the management of complex congenital heart lesions. Meticulous procedural planning through 3D modelling and simulation is vital to mitigate the risks of these innovative procedures.
永存左上腔静脉(LSVC)与左心房(LA)相连是一种罕见的异常情况,具有严重的临床意义。根据心内分流的血流方向,临床表现从发绀或反常栓塞到明显的右心衰竭不等。
一名26岁男性,婴儿期曾接受室间隔缺损(VSD)修复手术,现出现进行性运动不耐受症状。心脏成像显示,LSVC进入冠状窦(CS)上方的后壁有一个大的缺损,使LSVC与LA相连,导致肺静脉回流转向CS。所有肺静脉均正常连接至LA。大量的左向右心内分流导致显著的右心室扩张和三尖瓣反流。他接受了成功的解剖修复,通过经导管从LSVC到CS植入覆膜支架,将肺静脉回流重新导向LA。随访1年时,他的运动能力有所改善,心脏成像显示LSVC缺损完全封闭,肺静脉回流无梗阻。
据我们所知,我们的病例是首例报告这种不寻常的LSVC与LA连接的解剖变异,并通过经导管治疗进行完全修复的病例。先前关于其他形式的LSVC与LA连接的病例报告采用手术或装置封堵治疗,未对LSVC进行重新连接。该病例突出了创新的经皮技术在复杂先天性心脏病病变管理中的有效性和安全性。通过三维建模和模拟进行细致的手术规划对于降低这些创新手术的风险至关重要。