Attaran Robert R, Habibzadeh Mohammad R, Baweja Gurpreet, Slepian Marvin J
Sarver Heart Center, University of Arizona, Tucson, AZ 85724, USA.
Cardiovasc Pathol. 2009 Jan-Feb;18(1):49-52. doi: 10.1016/j.carpath.2007.07.012. Epub 2007 Oct 24.
Congenital quadricuspid aortic valves (QAVs) are rare phenomena. They are often associated with aortic insufficiency and significant morbidity. A QAV with an associated ascending aortic aneurysm is extremely rare, and these conditions might have a shared embryonic etiology. We describe the case of a patient with a QAV associated with aortic aneurysm. Pertinent literature on the QAV is reviewed, and embryological factors that may contribute to its pathogenesis are discussed.
先天性四叶式主动脉瓣(QAVs)是罕见现象。它们常与主动脉瓣关闭不全及严重发病情况相关。伴有升主动脉瘤的QAV极为罕见,并且这些情况可能有共同的胚胎学病因。我们描述了一例伴有主动脉瘤的QAV患者的病例。回顾了关于QAV的相关文献,并讨论了可能导致其发病机制的胚胎学因素。