Department of Pediatric Cardiology, Mackay Children's Hospital, Taipei City, Taiwan.
Department of Cardiology, Mackay Memorial Hospital, Taipei City, Taiwan.
Am J Case Rep. 2023 Jun 19;24:e939788. doi: 10.12659/AJCR.939788.
BACKGROUND Kawasaki disease (KD), a systemic vasculitis, affects children aged <5 years and is the leading acquired cardiovascular disease in developed countries. Although intravenous immunoglobulin is an effective treatment for KD and decreases the rate of cardiovascular complications, some patients still develop coronary sequelae, including coronary aneurysms and myocardial infarction. CASE REPORT A 9-year-old boy was diagnosed with KD at the age of 6 years. For coronary sequelae of a giant coronary artery aneurysm (CAA) 8.8 mm in diameter, he was prescribed aspirin and warfarin. At 9 years old, he visited the Emergency Department because of acute chest pain. Electrocardiography revealed an incomplete right bundle branch block and ST-T change over right and inferior leads. Also, troponin I was elevated. Coronary angiography found acute thrombotic occlusion of the right CAA. We performed aspiration thrombectomy with intravenous tirofiban. Coronary angiography and optical coherence tomography (OCT) images later found white thrombi, calcification, destruction of media layer, irregular intimal thickening, and uneven intima edge. We prescribed antiplatelet therapy and warfarin, and he was doing well at a 3-year follow-up. CONCLUSIONS OCT is a promising modality that can impact the clinical care in patients with coronary artery disease. This report presents treatment management and OCT images of KD complicated with a giant CAA and acute myocardial infarction. We used aspiration thrombectomy in combination with medical treatments as the initial intervention strategy. Afterward, the OCT images showed vascular wall abnormalities, which were helpful for defining the future risk and decision making of further coronary interventions and medical treatments.
川崎病(KD)是一种全身性血管炎,影响 5 岁以下儿童,是发达国家中主要的后天性心血管疾病。尽管静脉注射免疫球蛋白是治疗 KD 的有效方法,并降低了心血管并发症的发生率,但仍有部分患者发生冠状动脉后遗症,包括冠状动脉瘤和心肌梗死。
一名 9 岁男孩在 6 岁时被诊断为 KD。由于直径为 8.8 毫米的巨大冠状动脉瘤(CAA)的冠状动脉后遗症,他被开处阿司匹林和华法林。9 岁时,他因急性胸痛就诊于急诊。心电图显示不完全性右束支传导阻滞和右、下导联 ST-T 改变。肌钙蛋白 I 升高。冠状动脉造影发现右 CAA 急性血栓性闭塞。我们进行了抽吸血栓切除术联合静脉注射替罗非班。随后的冠状动脉造影和光学相干断层扫描(OCT)图像发现了白色血栓、钙化、中膜层破坏、内膜不规则增厚和不均匀的内膜边缘。我们开处了抗血小板治疗和华法林,在 3 年的随访中,他恢复良好。
OCT 是一种很有前途的方法,可以影响冠状动脉疾病患者的临床治疗。本报告介绍了伴有巨大 CAA 和急性心肌梗死的 KD 的治疗管理和 OCT 图像。我们使用抽吸血栓切除术联合药物治疗作为初始干预策略。随后的 OCT 图像显示血管壁异常,有助于确定未来的风险和决定进一步的冠状动脉介入和药物治疗。