Ogunleye Olushola O, Ajibola Oluwafemi, Cheema Mehmood, Oke Busala, Sperling Jason
Department of Internal Medicine, Vassar Brothers Medical Center, Poughkeepsie, USA.
Division of Cardiovascular Surgery, Vassar Brothers Medical Center, Poughkeepsie, USA.
Cureus. 2022 Jul 21;14(7):e27110. doi: 10.7759/cureus.27110. eCollection 2022 Jul.
Anomalous origin of the right coronary artery (ARCA) represents <3% of congenital coronary anomalies, while the subaortic membrane represents 6.5% of congenital heart anomalies. Symptomatic co-occurrence of ARCA and subaortic membrane in an adult is rare. A 68-year-old man developed a non-ST-elevation myocardial infarction necessitating percutaneous coronary intervention (PCI) four years prior to presentation at our hospital. In the years after his PCI, he developed progressive exertional breathlessness. Following a positive treadmill EKG, he underwent coronary CT angiography that indicated RCA dominance with ARCA arising from the left coronary sinus and coursing between the ascending aorta and pulmonary artery, causing 50-60% intraluminal narrowing at rest without atherosclerotic plaque. Echo showed normal left ventricular ejection fraction (LVEF) and a surprise finding of the subaortic membrane, with a modest gradient. He underwent successful resection of the subaortic membrane and unroofing of the anomalous RCA tunnel with tract marsupialization. The post-operative period was complicated by arrhythmias necessitating electrical cardioversion. At discharge, he was sent home on apixaban, bisoprolol, aspirin, atorvastatin, and an amiodarone taper. The subaortic membrane would not have required intervention independently because it was not associated with a severe gradient. However, surgery is recommended for symptomatic ARCA or subaortic membrane; hence, our patient underwent surgical management. Atrial fibrillation and flutter are the most common arrhythmias following cardiac surgery. Due to the patient's increased risk of complications, cardioversion and anticoagulation were pursued. Although ARCA is congenital, our patient had been asymptomatic for most of his life, suggesting that the development of the subaortic membrane might have triggered symptom onset, combining a modest subaortic gradient with previously asymptomatic exercise-induced right coronary ischemia. Clinicians should consider evaluating for secondary structural heart conditions in newly symptomatic adult patients with ARCA due to the risk of sudden cardiac death, to provide the most complete treatment.
右冠状动脉异常起源(ARCA)占先天性冠状动脉异常的比例不到3%,而主动脉下隔膜占先天性心脏异常的6.5%。成人中ARCA与主动脉下隔膜同时出现症状的情况很少见。一名68岁男性在我院就诊前四年发生了非ST段抬高型心肌梗死,需要进行经皮冠状动脉介入治疗(PCI)。在PCI后的几年里,他出现了进行性劳力性呼吸困难。在平板运动心电图呈阳性后,他接受了冠状动脉CT血管造影,结果显示右冠状动脉优势型,ARCA起源于左冠状窦,走行于升主动脉和肺动脉之间,静息时管腔内狭窄50%-60%,无动脉粥样硬化斑块。超声心动图显示左心室射血分数(LVEF)正常,意外发现主动脉下隔膜,有轻度压差。他成功地切除了主动脉下隔膜,并对异常的右冠状动脉隧道进行了开窗和袋形缝合术。术后出现心律失常,需要进行电复律。出院时,他带着阿哌沙班、比索洛尔、阿司匹林、阿托伐他汀和逐渐减量的胺碘酮回家。主动脉下隔膜本身不需要干预,因为它没有严重的压差。然而,对于有症状的ARCA或主动脉下隔膜,建议进行手术治疗;因此,我们的患者接受了手术治疗。心房颤动和扑动是心脏手术后最常见的心律失常。由于患者并发症风险增加,因此进行了复律和抗凝治疗。虽然ARCA是先天性的,但我们的患者一生中大部分时间都没有症状,这表明主动脉下隔膜的形成可能触发了症状的出现,将轻度的主动脉下压差与先前无症状的运动诱发的右冠状动脉缺血结合在一起。由于存在心脏性猝死的风险,临床医生应考虑对新出现症状的成年ARCA患者进行继发性结构性心脏病评估,以提供最全面的治疗。