Murray William, Lavery Ros, O'Brien Jim
Department of Cardiology, Mater Private Network, Eccles Street, Dublin D07WKW8, Ireland.
Eur Heart J Case Rep. 2023 Dec 23;8(1):ytad641. doi: 10.1093/ehjcr/ytad641. eCollection 2024 Jan.
Deviations from usual coronary artery anatomy are well documented. The left circumflex artery (LCx) arising from the pulmonary artery is an example of one such deviation which is rarely seen. We present the case of a 26-year-old male with this coronary artery distribution presenting with an episode of ventricular flutter with late gadolinium enhancement and pluri-morphological ventricular arrhythmias.
A 26-year-old male with a history of cardiac surgery presented to his local hospital with an episode of symptomatic broad-complex tachycardia (BCT). It failed to revert to sinus rhythm following intravenous beta-blockers and amiodarone and required external cardioversion. Subsequently, the patient developed a aspiration pneumonia requiring ICU admission, after which he was transferred to our institute for ongoing cardiac management. Cardiac computed tomography CTA and coronary angiography revealed that the LCx was found to originate from the pulmonary artery. He underwent insertion of a subcutaneous pacemaker and was subsequently discharged. Despite the potential for steal syndrome of viable coronary territories. Multidisciplinary team discussion determined him to be fit for conservative management and not for surgical correction of his anomalous coronary artery anatomy.
Aberrant coronary artery anatomy can lead to diverse outcomes for patients in terms of both morbidity and mortality. The need for surgery in these situations varies on a case-by-case basis and little research exists to guide decision-making for healthcare professionals. As such there is a need for further study both to guide treatment and to ensure high-quality outcomes for patients with this condition.
冠状动脉解剖结构异常已有充分记录。左旋支动脉(LCx)起源于肺动脉就是一种罕见的此类异常情况。我们报告一例26岁男性,其冠状动脉分布如此,出现了一次伴有延迟钆增强和多形性室性心律失常的室性心动过速发作。
一名有心脏手术史的26岁男性因一次有症状的宽QRS波心动过速(BCT)发作到当地医院就诊。静脉注射β受体阻滞剂和胺碘酮后未能恢复窦性心律,需要进行体外心脏复律。随后,患者发生吸入性肺炎,需要入住重症监护病房,之后被转至我院进行持续的心脏治疗。心脏计算机断层扫描CTA和冠状动脉造影显示,左旋支动脉起源于肺动脉。他接受了皮下起搏器植入,随后出院。尽管存在存活冠状动脉区域盗血综合征的可能性。多学科团队讨论决定他适合保守治疗,而不适合对其异常冠状动脉解剖结构进行手术矫正。
异常的冠状动脉解剖结构在发病率和死亡率方面可能给患者带来不同的后果。在这些情况下是否需要手术因具体病例而异,几乎没有研究可指导医疗专业人员的决策。因此,需要进一步研究以指导治疗并确保患有这种疾病的患者获得高质量的治疗效果。