Khan Shamruz Khan Akerem, Tamin Syahidah Syed, Araoz Philip A
Department of Radiology, Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA.
J Comput Assist Tomogr. 2011 Sep-Oct;35(5):637-41. doi: 10.1097/RCT.0b013e318224a129.
Quadricuspid aortic valve (QAV) is a rare congenital cardiac entity. The recognition of QAV has clinical significance as it causes aortic valve dysfunction, commonly aortic regurgitation, and is often associated with other congenital cardiac abnormalities. We showed the important role played by cardiac magnetic resonance imaging in detecting QAV and review the available literature to explain its incidence, diagnosis, classifications, embryology, correlation between morphology of the QAV and its function, associated conditions, and management.
四叶式主动脉瓣(QAV)是一种罕见的先天性心脏疾病。认识QAV具有临床意义,因为它会导致主动脉瓣功能障碍,常见的是主动脉瓣反流,并且常与其他先天性心脏异常相关。我们展示了心脏磁共振成像在检测QAV中所起的重要作用,并回顾现有文献以解释其发病率、诊断、分类、胚胎学、QAV形态与其功能之间的相关性、相关病症及治疗。