Jaglan Akshar, Ajam Tarek, Port Steven C, Bajwa Tanvir, Tajik A Jamil
Aurora Cardiovascular Services, Aurora Sinai/Aurora St. Luke's Medical Centers, 2801 W. Kinnickinnic River Parkway, Ste. 880, Milwaukee, WI 53215, USA.
Eur Heart J Case Rep. 2020 Nov 18;4(6):1-5. doi: 10.1093/ehjcr/ytaa274. eCollection 2020 Dec.
Coronary artery ectasia (CAE) is a rare anomaly that can present at any age. Predisposing risk factors include Kawasaki disease in a younger population and atherosclerosis in the older generation. We present a unique case of the management of a young woman diagnosed with multivessel CAE with aneurysmal changes in the setting of acute coronary syndrome and subsequently during pregnancy.
A 23-year-old woman presented with acute onset chest pain. Electrocardiogram revealed no ischaemic changes; however, troponin I peaked at 16 ng/mL (reference range 0-0.04 ng/mL). Echocardiogram showed apical dyskinesis with preserved left ventricular ejection fraction. Coronary angiography showed multivessel CAE along with significant thrombus burden in an ectatic lesion of the left anterior descending artery. Since the patient was haemodynamically stable, conservative management with dual antiplatelet therapy and anticoagulation was started. On follow-up, coronary computed tomographic angiogram illustrated resolution of the coronary thrombi and echocardiogram showed improvement to the apical dyskinesis. It was presumed that Kawasaki disease was the most likely aetiology of her disease. Subsequently the patient reported that, contrary to medical advice, she was pregnant, adding another layer of complexity to her case.
Coronary artery ectasia can be discovered as an incidental finding or can present with an acute coronary syndrome. Management is challenging in the absence of randomized trials and large-scale data. Treatment options include medications, percutaneous intervention, and surgical revascularization. Close surveillance is required in these patients to assess progression of disease. Here we discuss treatment options during acute coronary syndrome and pregnancy.
冠状动脉扩张(CAE)是一种罕见的异常情况,可在任何年龄出现。易感风险因素包括年轻人群中的川崎病和老年人群中的动脉粥样硬化。我们报告了一例年轻女性多支冠状动脉扩张合并动脉瘤样改变的独特病例,该病例发生在急性冠状动脉综合征背景下,随后在妊娠期间。
一名23岁女性因急性胸痛就诊。心电图显示无缺血性改变;然而,肌钙蛋白I峰值达到16 ng/mL(参考范围0 - 0.04 ng/mL)。超声心动图显示心尖运动障碍,左心室射血分数保留。冠状动脉造影显示多支冠状动脉扩张,同时左前降支动脉扩张病变处有大量血栓负荷。由于患者血流动力学稳定,开始采用双重抗血小板治疗和抗凝进行保守治疗。随访时,冠状动脉计算机断层血管造影显示冠状动脉血栓溶解,超声心动图显示心尖运动障碍有所改善。推测川崎病最有可能是其病因。随后患者报告称,与医嘱相反,她怀孕了,这使她的病例更加复杂。
冠状动脉扩张可作为偶然发现,也可表现为急性冠状动脉综合征。在缺乏随机试验和大规模数据的情况下,管理具有挑战性。治疗选择包括药物治疗、经皮介入治疗和外科血管重建。这些患者需要密切监测以评估疾病进展。在此我们讨论急性冠状动脉综合征和妊娠期间的治疗选择。