Vicol C, Rupp G, Struck E
Herzchirurgische Klinik, Zentralklinikum Augsburg.
Z Kardiol. 1997 Jul;86(7):538-40. doi: 10.1007/s003920050091.
We report on a 61-year-old patient with considerable insufficiency of a quadricuspid aortic valve and coronary three vessel disease. The congenital quadricuspid aortic valve has become symptomatic due to the development of (post-endocarditic) insufficiency only in the advanced stage of life. It was treated by replacement of the aortic valve and bypass myocardial revascularization. The physiopathology of quadricuspid aortic valve will be discussed.
我们报告了一例61岁患者，患有严重的四叶式主动脉瓣功能不全和冠状动脉三支血管病变。先天性四叶式主动脉瓣仅在生命晚期因（心内膜炎后）功能不全的发展而出现症状。通过主动脉瓣置换和旁路心肌血运重建进行了治疗。将讨论四叶式主动脉瓣的生理病理学。
