Omuro Ayumi, Matsuyama Tetsuya, Okada Seigo, Okamura Takayuki
Department of Medicine and Clinical Science, Division of Cardiology, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
Department of Pediatrics, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
J Cardiol Cases. 2024 Jan 15;29(4):197-200. doi: 10.1016/j.jccase.2023.12.011. eCollection 2024 Apr.
A 34-year-old man with a history of Kawasaki disease had been experiencing chest pain at rest since middle school. Multidetector-row computed tomography showed no aneurysm formation; however, the right coronary artery had an anomalous origin with moderate stenosis. Invasive coronary angiography revealed moderate right coronary artery stenosis with a fractional flow reserve of 0.97. Finally, with a positive acetylcholine provocation test and elevated index of microvascular resistance, the patient was diagnosed with microvascular and epicardial vasospastic angina in the endotypes of ischemia with nonobstructive coronary arteries. This is the first reported case of both microvascular and epicardial vasospastic angina after Kawasaki disease. In patients with a history of Kawasaki disease, even those without cardiac sequelae, coronary endothelial and microvascular dysfunctions should be taken into consideration.
We report the first case of both microvascular and epicardial vasospastic angina in the endotypes of ischemia with nonobstructive coronary arteries after Kawasaki disease.Coronary endothelial and microvascular dysfunctions should be taken into consideration in patients with a history of Kawasaki disease, even those without cardiac sequelae.
一名34岁有川崎病病史的男性自中学起就一直经历静息性胸痛。多排螺旋计算机断层扫描显示无动脉瘤形成;然而,右冠状动脉起源异常并伴有中度狭窄。有创冠状动脉造影显示右冠状动脉中度狭窄,血流储备分数为0.97。最后,由于乙酰胆碱激发试验阳性且微血管阻力指数升高,该患者最终被诊断为非阻塞性冠状动脉缺血亚型中的微血管性和心外膜血管痉挛性心绞痛。这是首例报道的川崎病后同时出现微血管性和心外膜血管痉挛性心绞痛的病例。对于有川崎病病史的患者,即使没有心脏后遗症,也应考虑冠状动脉内皮和微血管功能障碍。
我们报告了首例川崎病后非阻塞性冠状动脉缺血亚型中同时出现微血管性和心外膜血管痉挛性心绞痛的病例。对于有川崎病病史的患者,即使没有心脏后遗症,也应考虑冠状动脉内皮和微血管功能障碍。