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Anomalous origin of left main coronary artery from the right sinus of Valsalva presenting as non ST elevation acute coronary syndrome: A case report

机译:瓦尔萨尔瓦州右窦的左主冠状动脉异常起源为非ST段抬高的急性冠状动脉综合征:一例报告

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摘要

Congenital anomalies of the coronary arteries are a cause of sudden cardiac death. Of the known anatomic variants, anomalous origination of a coronary artery from an opposite sinus of Valsalva (ACAOS) remains a major clinical issue and a challenging condition to treat. Congenital coronary anomalies are likely to be under-recognized, as completing an anatomic assessment in a very large portion of the population would seem unfeasible. However, we present a case report with image of a 49 year old male presented with acute non-ST elevation ACS for which he underwent diagnostic angiography of the coronary system which revealed a common origin of both right and left main coronary artery from right sinus of Valsalva with significant obstructive lesion in the mid segment of right coronary artery. However, due to financial constraints CT angiography could not be done in this patient to identify the detail anatomy and the course of the anomalous left coronary artery origin (L-ACAOS). He was managed medically with dual antiplatelets, beta blockers, nitrates and ACE inhibitors.
机译:冠状动脉的先天性异常是心脏猝死的原因。在已知的解剖学变异中,冠状动脉异常起源于瓦尔萨尔瓦的对侧窦(ACAOS)仍然是主要的临床问题,也是治疗的挑战性条件。先天性冠状动脉畸形很可能未被充分认识,因为在很大一部分人口中完成解剖学评估似乎是不可行的。但是,我们提供了一个病例报告,其中有一名49岁男性患有急性非ST段抬高ACS,他接受了冠状动脉系统的诊断性血管造影,显示了右主动脉和左主动脉的共同起源于右鼻窦右冠状动脉中段有明显的梗阻性病变。但是,由于经济上的限制,该患者无法进行CT血管造影以识别详细的解剖结构和左冠状动脉起源异常(L-ACAOS)的过程。他曾接受双重抗血小板,β受体阻滞剂,硝酸盐和ACE抑制剂的药物治疗。

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