Barik Ramachandra, Acharya Debasis, Deb Pranjit, Panda Debasis, Malla Sindhu Rao
Cardiology, All India Institute of Medical Sciences, Bhubaneswar, Bhubaneswar, IND.
Cureus. 2025 Feb 21;17(2):e79395. doi: 10.7759/cureus.79395. eCollection 2025 Feb.
Trilogy of Fallot is a rare congenital heart disease consisting of pulmonary stenosis, right-to-left interatrial shunt, and right ventricular hypertrophy. It can lead to complications such as thrombus formation as a result of chronic hypoxia leading to erythrocytosis and hyperviscosity, and paradoxical embolisms due to the right-to-left interatrial shunt. This report illustrates a case of a young man who presented with cyanosis and right heart failure with a history of recurrent episodes of transient ischemic attacks. He was found to have Trilogy of Fallot with a large right atrial thrombus. He showed significant improvement following treatment with low molecular weight heparin and thereafter undergoing balloon pulmonary valvotomy.
法洛三联症是一种罕见的先天性心脏病,由肺动脉狭窄、心房右向左分流和右心室肥厚组成。它可导致并发症,如由于慢性缺氧导致红细胞增多症和高粘滞血症而形成血栓,以及由于心房右向左分流导致反常栓塞。本报告阐述了一例年轻男性病例,该患者有发绀和右心衰竭症状,并有短暂性脑缺血发作反复发作史。他被诊断为法洛三联症并伴有巨大右心房血栓。在接受低分子量肝素治疗并随后进行球囊肺动脉瓣切开术后,他的病情有了显著改善。