Wong Christopher C Y, Pogatchnik Brian P, Clark Daniel E, Sharma Rahul P
Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Department of Radiology, Stanford University School of Medicine, Stanford, CA, USA.
Eur Heart J Case Rep. 2024 Apr 15;8(4):ytae192. doi: 10.1093/ehjcr/ytae192. eCollection 2024 Apr.
Anomalous aortic origin of a coronary artery from the opposite sinus is a rare congenital abnormality that may be encountered during primary percutaneous coronary intervention (PCI) for ST-elevation myocardial infarction (STEMI).
A 65-year-old man presented with chest pain and signs of heart failure. Electrocardiogram demonstrated atrial fibrillation with ST elevation in the high lateral leads, and he was taken emergently to the cardiac catheterization laboratory for primary PCI. Coronary angiography identified the culprit to be an occluded anomalous left main coronary artery (LMCA) arising from the right coronary cusp, and primary PCI was successfully performed in the LMCA and the left anterior descending artery (LAD). Computed tomography angiography confirmed a benign retroaortic course of the anomalous LMCA with no additional high-risk features, as well as a new left atrial appendage thrombus. He subsequently developed deep venous thrombosis, acute pulmonary embolism, and acute kidney injury secondary to renal artery embolism with associated infarction. Workup for patent foramen ovale and thrombophilia were negative, and he was discharged in a stable condition. At 2-month follow-up, he was asymptomatic with no evidence of myocardial ischaemia on stress cardiac magnetic resonance imaging.
We present the first reported case of an occluded anomalous LMCA arising from the right coronary sinus in a patient presenting with STEMI. Rapid recognition of this congenital anomaly and selection of an appropriate guide catheter were keys to achieving timely reperfusion and a good outcome in this case.
冠状动脉从对侧窦异常起源是一种罕见的先天性异常,在ST段抬高型心肌梗死(STEMI)的初次经皮冠状动脉介入治疗(PCI)过程中可能会遇到。
一名65岁男性因胸痛和心力衰竭症状就诊。心电图显示高侧壁导联ST段抬高伴心房颤动,他被紧急送往心脏导管室进行初次PCI。冠状动脉造影确定罪犯血管为起源于右冠状动脉窦的闭塞性异常左主干冠状动脉(LMCA),并在LMCA和左前降支(LAD)成功进行了初次PCI。计算机断层扫描血管造影证实异常LMCA走行于主动脉后方为良性,无其他高危特征,同时发现一个新的左心耳血栓。他随后发生了深静脉血栓形成、急性肺栓塞以及继发于肾动脉栓塞伴梗死的急性肾损伤。卵圆孔未闭和易栓症检查均为阴性,他出院时病情稳定。在2个月的随访中,他无症状,负荷心脏磁共振成像未显示心肌缺血证据。
我们报告了首例STEMI患者中起源于右冠状动脉窦的闭塞性异常LMCA病例。快速识别这种先天性异常并选择合适的引导导管是该病例实现及时再灌注和良好预后的关键。