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伴有升主动脉瘤的四叶式主动脉瓣:一例报告及胚胎学机制探讨

Quadricuspid aortic valve with ascending aortic aneurysm: report of a case and discussion of embryological mechanisms.

作者信息

Attaran Robert R, Habibzadeh Mohammad R, Baweja Gurpreet, Slepian Marvin J

机构信息

Sarver Heart Center, University of Arizona, Tucson, AZ 85724, USA.

出版信息

Cardiovasc Pathol. 2009 Jan-Feb;18(1):49-52. doi: 10.1016/j.carpath.2007.07.012. Epub 2007 Oct 24.

Abstract

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.

摘要

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。

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