Anomalous origin of left main coronary artery from the right sinus of Valsalva

IF 2.3 3区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS BMC Cardiovascular Disorders Pub Date : 2023-12-14 DOI:10.1186/s12872-023-03616-x
Frederick Chua, Kenny Vongbunyong, Deniz Akay Urgun, Roxana Ghashghaei
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Abstract

Anomalous coronary arteries are rare congenital variations with cases ranging from asymptomatic to life-threatening. Given the wide variability of coronary anomalies, it is challenging to predict their clinical consequences. Here, we present the ‘malignant’ variant – interarterial course of the left coronary artery between the aorta and pulmonary trunk – given the highest risk of sudden cardiac death among the various coronary anomalies. Our case presents a 22-year-old male presenting to the emergency department after a syncopal episode that occurred while the patient was driving a motor vehicle. Initial Computed Tomography (CT) of the chest performed as part of the trauma work-up revealed a rare case of an anomalous origin of the left main coronary artery (LMCA) originating from a common ostium with the right coronary artery (RCA). The LMCA was found to have a malignant course, as it was positioned between the aorta and pulmonary artery. Given the high risk of sudden cardiac arrest with this congenital variant, the patient underwent coronary artery bypass grafting. Anomalous coronary arteries remain the second leading cause of sudden cardiac death in young adult patients. The risk of sudden cardiac death depends on the congenital variant of the anomalous coronary artery as well as the course these vessels take. This case highlights a rare congenital variant featuring both the LMCA and RCA originating from a common ostium, with the LMCA having a malignant course, a variant with the highest risk of sudden cardiac death.
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左冠状动脉主干异常起源于瓦尔萨尔瓦右窦
冠状动脉异常是一种罕见的先天性变异,病例从无症状到危及生命不等。由于冠状动脉异常的变异性很大,预测其临床后果具有挑战性。在此,我们介绍了 "恶性 "变异--左冠状动脉在主动脉和肺动脉干之间的动脉间走向--在各种冠状动脉畸形中发生心脏性猝死的风险最高。我们的病例是一名 22 岁的男性,在驾驶机动车时突发晕厥,随后被送往急诊科。作为创伤检查的一部分,初步胸部计算机断层扫描(CT)显示,左冠状动脉主干(LMCA)起源异常,与右冠状动脉(RCA)共用一个骨膜,这种情况非常罕见。由于 LMCA 位于主动脉和肺动脉之间,因此发现它的走向是恶性的。鉴于这种先天性变异极易导致心脏骤停,患者接受了冠状动脉搭桥术。冠状动脉异常仍然是年轻成人患者心脏性猝死的第二大原因。心脏性猝死的风险取决于异常冠状动脉的先天变异以及这些血管的走向。本病例突出显示了一种罕见的先天性变异,即 LMCA 和 RCA 均起源于一个共同的骨膜,其中 LMCA 走向恶性,这种变异导致心脏性猝死的风险最高。
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来源期刊
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.50
自引率
0.00%
发文量
480
审稿时长
1 months
期刊介绍: BMC Cardiovascular Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the heart and circulatory system, as well as related molecular and cell biology, genetics, pathophysiology, epidemiology, and controlled trials.
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