Saito Tetsuya, Kawamura Masashi, Murakami Takashi, Sakaki Masayuki
Department of Cardiovascular Surgery, National Hospital Organization Osaka National Hospital, 2-1-14 Hoenzaka, Chuo-ku, Osaka 540-0006, Japan.
Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.
Eur Heart J Case Rep. 2023 Sep 11;7(9):ytad459. doi: 10.1093/ehjcr/ytad459. eCollection 2023 Sep.
Bicuspid aortic valve (BAV) with displacement of the attachment of the conjoined aortic leaflet and fibrous strands is a rare cardiac malformation. We report a case of BAV that presented as acute massive aortic regurgitation during cardiopulmonary bypass for a planned non-valve-related procedure and was successfully treated by emergency aortic valve replacement.
A 70-year-old man with triple vessel coronary disease and severe left ventricular systolic dysfunction underwent coronary bypass grafting and graft replacement of the ascending aorta. Acute aortic regurgitation occurred during ventricular fibrillation and after de-clamping of the aortic graft. Intra-operative findings included a fused BAV (right-left cusp fusion), very asymmetrical leaflet (commissure angle of the non-fused leaflet 135°), three aortic sinuses, and conjoined leaflets originating from the myocardium in the inter-ventricular septum. The aortic leaflets were resected and replaced with a prosthetic aortic valve at the attachment site of the conjoined leaflets. Post-operatively, no peri-valvular leaks were observed, and left ventricular function was improved.
Intra-operative acute massive aortic regurgitation may be caused by a morphologically abnormal aortic leaflet and root complex in patients with a BAV. The dilated aortic root, asymmetrical leaflet, and abnormal aortic leaflet insertion, with thick septal myocardium of the coronary aortic sinus, might have caused unstable leaflet co-aptation, leading to deformation of the aortic leaflets influenced by the change in myocardial tone and intra-operative change in the sinotubular junction. Familiarity with the classification of congenital BAV, and the anatomy of the normal and abnormal aortic root complex, is important.
伴有联合主动脉瓣叶附着移位及纤维条索的二叶式主动脉瓣(BAV)是一种罕见的心脏畸形。我们报告一例BAV病例,该病例在计划进行非瓣膜相关手术的体外循环期间表现为急性大量主动脉瓣反流,并通过紧急主动脉瓣置换术成功治疗。
一名患有三支血管冠状动脉疾病和严重左心室收缩功能障碍的70岁男性接受了冠状动脉搭桥术和升主动脉移植置换术。在心室颤动期间及主动脉移植血管松开后发生了急性主动脉瓣反流。术中发现包括融合的BAV(右-左瓣叶融合)、非常不对称的瓣叶(未融合瓣叶的瓣叶角为135°)、三个主动脉窦以及起源于室间隔心肌的联合瓣叶。在联合瓣叶的附着部位切除主动脉瓣叶并用人工主动脉瓣进行置换。术后未观察到瓣周漏,左心室功能得到改善。
BAV患者术中急性大量主动脉瓣反流可能由形态异常的主动脉瓣叶和根部复合体引起。扩张的主动脉根部、不对称的瓣叶以及异常的主动脉瓣叶插入,伴有冠状动脉主动脉窦增厚的间隔心肌,可能导致瓣叶对合不稳定,导致主动脉瓣叶受心肌张力变化和术中窦管交界处变化的影响而变形。熟悉先天性BAV的分类以及正常和异常主动脉根部复合体的解剖结构很重要。