Sivri Serkan, Bastug Serdal, Can Guney Murat, Alsancak Yakup, Ozdemir Elcin, Bozkurt Engin
Ahi Evran University Education and Research Hospital, Division of Cardiology, Kırşehir, Turkey. Electronic correspondence:
Atatürk Education and Research Hospital, Division of Cardiology, Ankara, Turkey.
J Heart Valve Dis. 2017 Mar;26(2):243-246.
The quadricuspid aortic valve (QAV) is a very uncommon congenital malformation with an estimated incidence of 0.003% to 0.043% of all congenital heart diseases. Combinations of QAV with several different congenital malformations have been described. The case is reported of a type A QAV associated with moderate aortic regurgitation, mild mitral regurgitation, and ascending aorta dilatation. This interesting case was referred for close follow up.
四叶式主动脉瓣（QAV）是一种非常罕见的先天性畸形，在所有先天性心脏病中估计发病率为0.003%至0.043%。已有QAV与几种不同先天性畸形合并存在的报道。本文报告了1例A型QAV合并中度主动脉瓣反流、轻度二尖瓣反流及升主动脉扩张的病例。该有趣病例被转诊以进行密切随访。
