巨主动脉弓动脉瘤合并川崎病1例报告。

Cardiologie tunisienne Pub Date : 2013-01-01
Hakim Kaouthar, Boussaada Rafik, Ayari Jihen, Hamdi Imen, Chaker Lilia, Ouarda Fatma, Msaad Hela
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引用次数: 0

摘要

川崎病(Kawasaki disease, KD)是一种儿科常见的急性血管炎,通常累及中小动脉,通常是冠状动脉。虽然KD后冠状动脉瘤的发生率和自然病程有很好的文献记载,但有关外周动脉和主动脉瘤的相关报道很少。我们报告一位28个月大的病患,诊断为川崎病,并发巨动脉瘤累及主动脉弓的水平部份。由于机械并发症和破裂的风险,这种并发症在开始时采用类固醇治疗,而不是手术。
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Giant aortic arch aneurysm complicating Kawasaki disease: an original case report.

Kawasaki disease (KD) is a common acute vasculitis in pediatric population that usually involves small and middle-sized arteries, commonly coronary arteries. Although the incidence and natural course of coronary aneurysms after KD are well documented, related reports on peripheral arterial and aortic aneurysms are scarce. We report an original case of a giant aortic aneurysm involving the horizontal part of aortic arch in a 28 months- old patient diagnosed with Kawasaki Disease. This complication was managed by steroids therapy in the beginning than surgery was indicated because of mechanical complication and risk of rupture.

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[Circular shunt in the severe neonatal form of Ebstein's Anomaly. The prostaglandine infusion is it beneficial or harmful?] Giant aortic arch aneurysm complicating Kawasaki disease: an original case report. Cardiac anomalies in Cantrell's pentalogy: From ventricular diverticulum to complete thoracic ectopia cordis.
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