A Rare Variant of an Anomalous Origin of the Left Coronary Artery, the Great Masquerader of Angina?

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Abstract

Anomalous aortic origin of the coronary arteries (AAOCA) is a rare set of anatomical variants that can present with symptoms such as angina and dyspnea on exertion with complications including acute coronary syndrome and sudden cardiac death. This case demonstrates a patient presenting with classic anginal symptoms with an incidental finding of one of the rarest variants and its complexity in cannulation: a left main coronary artery arising from the non-coronary cusp. Despite insignificant left coronary disease on coronary angiography, we had a high index of suspicion for underlying coronary vasospasm as a major contributor to her recurrent symptoms. AAOCA is an anatomical finding that warrants clinician awareness and close follow-up with recommendation for surgery if symptomatic.
左冠状动脉异常起源的罕见变异,心绞痛的大假面犯?
冠状动脉异常主动脉起源(AAOCA)是一组罕见的解剖变异,可表现为心绞痛和呼吸困难等症状,并伴有急性冠状动脉综合征和心源性猝死等并发症。本例患者表现出典型的心绞痛症状,在插管时偶然发现一种最罕见的变异及其复杂性:从非冠状动脉尖端产生的左冠状动脉主干。尽管冠状动脉造影显示左冠状动脉病变不明显,但我们高度怀疑潜在的冠状动脉血管痉挛是她复发症状的主要原因。AAOCA是一种解剖学发现,值得临床医生注意并密切随访,如果有症状,建议手术治疗。
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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