Congenital Coronary Artery Anomalies: Three Cases and Brief Review of the Literature.

Case Reports in Vascular Medicine Pub Date : 2021-01-30 eCollection Date: 2021-01-01 DOI:10.1155/2021/6612289
Nikolaos S Ioakeimidis, Dimitrios Valasiadis, Andreas Markou, Theodora Zaglavara
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Abstract

Coronary artery anomalies (CAAs) are congenital vascular defects which can remain hidden and asymptomatic over the complete life course of an individual. They are defined as deviations from the normal coronary anatomy regarding the arterial origin, course, or both. Their incidence varies from 1.3% to 5.64% in coronary angiography cohorts, and they can be detected as incidental findings. In certain cases, CAAs can be hemodynamically significant and unfortunately can be proven lethal. Their link with sudden cardiac death, especially in otherwise healthy competitive athletes, is well established, but their prognostic significance, range of symptoms, and pathophysiology remain to be further elucidated. Here, along with a brief review of related literature, we present a series of three cases: one case of an anomalous origin of the right coronary artery (RCA) from the left coronary sinus, one case of a split RCA originating from the left coronary sinus, and one case of a dual left anterior descending (LAD) artery system.

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先天性冠状动脉异常3例及文献复习。
冠状动脉异常(CAAs)是一种先天性血管缺陷,可以在个体的整个生命过程中保持隐匿和无症状。它们被定义为与正常冠状动脉解剖结构在动脉起源、路线或两者上的偏离。在冠状动脉造影队列中,它们的发病率从1.3%到5.64%不等,它们可以作为偶然发现被检测出来。在某些情况下,CAAs可能具有血流动力学意义,不幸的是可能被证明是致命的。它们与心源性猝死的联系,尤其是在其他方面健康的竞技运动员中,已经得到了很好的证实,但它们的预后意义、症状范围和病理生理学仍有待进一步阐明。在此,我们对相关文献进行了简要的回顾,并提出了一系列的三个病例:一例右冠状动脉(RCA)起源于左冠状动脉窦的异常起源,一例起源于左冠状动脉窦的分裂RCA,以及一例双左前降支(LAD)动脉系统。
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审稿时长
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