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先天性主动脉瓣异常。伴有左冠状动脉孤立的主动脉瓣关闭不全。

Congenital aortic valve anomaly. Aortic regurgitation with left coronary artery isolation.

作者信息

Line D E, Babb J D, Pierce W S

出版信息

J Thorac Cardiovasc Surg. 1979 Apr;77(4):533-5.

PMID:154598
Abstract

A case is reported of aortic regurgitation resulting from a congenitally abnormal aortic valve. The left coronary cusp of the valve was small and adhered to the aortic wall, so that there was insufficient valve tissue to maintain diastolic valve competence. In addition, this rudimentary cusp completely occluded the left coronary ostium. The patient was treated successfully by valve replacement.

摘要

报告一例因先天性主动脉瓣异常导致主动脉瓣反流的病例。该瓣膜的左冠状动脉瓣叶较小且与主动脉壁粘连,以至于没有足够的瓣膜组织来维持舒张期瓣膜功能。此外,这个发育不全的瓣叶完全阻塞了左冠状动脉口。患者通过瓣膜置换术获得成功治疗。

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J Thorac Cardiovasc Surg. 1979 Apr;77(4):533-5.
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引用本文的文献

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Heart Rate Induced Dynamic Coronary Ischemia Secondary to Aortic Valve Insufficiency from a Diminutive Aortic Valve Leaflet: Diagnosis and Repair.因小型主动脉瓣叶导致主动脉瓣关闭不全引起的心率诱导性动态性冠状动脉缺血:诊断与修复。
Pediatr Cardiol. 2022 Mar;43(3):691-694. doi: 10.1007/s00246-021-02772-1. Epub 2021 Nov 24.
2
Surgical repair of congenital aortic regurgitation by aortic root reduction: A finite element study.通过主动脉根部缩窄术对先天性主动脉瓣反流进行手术修复:一项有限元研究。
J Biomech. 2015 Nov 5;48(14):3883-9. doi: 10.1016/j.jbiomech.2015.09.030. Epub 2015 Oct 3.
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Dysplastic aortic cusp presenting with myocardial ischemia: diagnostic value of transesophageal echocardiography.
Int J Cardiovasc Imaging. 2005 Apr-Jun;21(2-3):219-23. doi: 10.1007/s10554-004-2977-6.
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Congenital valvar aortic stenosis and abnormal origin of the right coronary artery: rare combination with important clinical implications.先天性瓣膜性主动脉狭窄与右冠状动脉异常起源:罕见组合,具有重要临床意义。
Pediatr Cardiol. 1995 Mar-Apr;16(2):73-5. doi: 10.1007/BF00796821.
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Congenital aortic regurgitation in a child with a tricuspid non-stenotic aortic valve.一名患有三尖瓣无狭窄主动脉瓣的儿童的先天性主动脉瓣反流。
Br Heart J. 1984 Mar;51(3):358-60. doi: 10.1136/hrt.51.3.358.
6
Coronary artery obstruction associated with congenital aortic valve disease.与先天性主动脉瓣疾病相关的冠状动脉阻塞。
Br Heart J. 1984 Nov;52(5):585-7. doi: 10.1136/hrt.52.5.585.