Bicuspid aortic valve with dissecting aortic aneurysm in an African

E. Ogbemudia, A. Ogbomo
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引用次数: 0

Abstract

Bicuspid aortic valve (BAV) is a relatively rare congenital heart disease (CHD) in Africans compared to caucasians and it is an independent risk factor for aortic aneurysm and dissection. We therefore report a case of a 51-year old farmer who presented with clinical features of heart failure (HF). He had a diastolic murmur loudest in the aortic area. Echocardiography revealed BAV with regurgitation. The aortic root and ascending aorta were dilated with dissection flaps which mimicked a double aortic valve. Computed Tomography angiography of the aorta confirmed Debakey’s type 1 (Stanford A) dissecting aortic aneurysm (DAA). He was managed for HF due to chronic aortic regurgitation and referred for surgery. BAV is a relatively rare CHD in Africans and is a strong risk factor for DAA. Long-term monitoring of the aorta and timely surgical intervention are recommended when indicated.
非洲人二尖瓣主动脉瓣伴夹层主动脉瘤
与高加索人相比,非洲人的双尖瓣主动脉瓣(BAV)是一种相对罕见的先天性心脏病(CHD),是导致主动脉瘤和夹层的独立危险因素。因此,我们报告了一例51岁的农民,他表现出心力衰竭(HF)的临床特征。他在主动脉区有最大的舒张期杂音。超声心动图显示BAV伴返流。用夹层皮瓣模拟双主动脉瓣扩张主动脉根和升主动脉。计算机断层血管造影证实Debakey 1型(Stanford A)夹层主动脉瘤(DAA)。由于慢性主动脉反流,他被诊断为心衰,并转介手术。在非洲,BAV是一种相对罕见的冠心病,是DAA的重要危险因素。如有需要,建议长期监测主动脉并及时进行手术干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
7 weeks
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