以主动脉不全为首发表现的Takayasu动脉炎1例报告

A. Fadoul Tahir, K. Badaoui, A. Boucetta, S. Abouradi, A. Assklou, M. Haboub, S. Arous, M. G. Bennouna, A. Drighil, L. Azzouzi, R. Habbal
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引用次数: 0

摘要

高须病是年轻人炎症性主动脉炎的首要病因。这种疾病主要影响妇女。高松病可能是主动脉对各种感染性或免疫功能障碍病因的一种非特异性反应模式。7 - 10%的病例存在主动脉功能不全。它通常是温和的。其机制并不明确:直接损害主动脉瓣或扩张主动脉环。引起心绞痛甚至心肌梗塞的冠状动脉损伤也是可能的。我们报告一例严重的主动脉不全继发于高松病并发急性冠状动脉综合征在一个42岁的妇女。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Takayasu's Arteritis with Aortic Insufficiency as Initial Presentation: A Case Report
Takayasu's disease is the first cause of inflammatory aortitis in young subjects. The disease preferentially affects the women. Takayasu's disease could be a mode of non-specific reaction of the aorta to various infectious or dysimmune etiological factors. Aortic insufficiency is present in 7 to 10% of cases. It is usually moderate. Its mechanism is not unambiguous: direct damage to the aortic valves or dilation of the aortic annulus. Coronary damage responsible for angina or even myocardial infarction are also possible. We report the case of a severe aortic insufficiency secondary to takayasu disease complicated by acute coronary syndrome in a 42-year-old woman.
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