Cardiovascular Surgery Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
J Cardiothorac Surg. 2024 Sep 12;19(1):526. doi: 10.1186/s13019-024-02985-4.
Congenital Quadricuspid Aortic Valve (QAV) malformation is a relatively rare cardiac valve malformation, especially with abnormal coronary opening and severe stenosis of Coronary Artery Disease (CAD). The patient underwent "one-stop" interventional treatment with transcatheter aortic valve replacement and percutaneous coronary stent implantation. Follow up for 12-month with good outcomes.
先天性四叶式主动脉瓣(QAV)畸形是一种相对罕见的心脏瓣膜畸形,特别是伴有异常冠状动脉开口和严重冠状动脉疾病(CAD)狭窄的患者。该患者接受了经导管主动脉瓣置换术和经皮冠状动脉支架植入术的“一站式”介入治疗。随访 12 个月,结果良好。