Sliem Ashraf, Siu Alfonso, Zheng Jin, Magana Sergio, Alagha Zakaria, Ghallab Muhammad, Lopez Manuel
Internal Medicine, Flushing Hospital Medical Center, Flushing, USA.
Internal Medicine, Marshall University Joan C. Edwards School of Medicine, West Virginia, USA.
Cureus. 2023 Jun 23;15(6):e40855. doi: 10.7759/cureus.40855. eCollection 2023 Jun.
Kawasaki Disease (KD) is a self-limited acute vasculitis that mainly affects medium-sized arteries in childhood, with the coronary arteries being one of the main targets. A well-known complication is a coronary aneurysm with myocardial ischemia. We report the case of a 29-year-old female with an insignificant past medical history who presented with sudden cardiac arrest. Labs were significant for elevated troponin, consistent with non-ST elevation myocardial infarction, given diffuse ST depression on the electrocardiogram. The patient underwent a coronary angiogram that revealed diffuse coronary artery disease with multiple ulcerations, aneurysms, and occlusions consistent with KD, despite denying prior history. Cardiac arrest may be the initial presentation of undiagnosed KD and should be considered as one of the differential diagnoses.
川崎病(KD)是一种自限性急性血管炎,主要影响儿童期的中等大小动脉,冠状动脉是主要受累部位之一。一个众所周知的并发症是冠状动脉瘤伴心肌缺血。我们报告一例29岁女性病例,其既往病史无特殊,现突发心脏骤停。实验室检查显示肌钙蛋白升高,与非ST段抬高型心肌梗死相符,心电图显示弥漫性ST段压低。尽管患者否认既往病史,但冠状动脉造影显示弥漫性冠状动脉疾病,伴有多处溃疡、动脉瘤和闭塞,符合川崎病表现。心脏骤停可能是未诊断出的川崎病的首发表现,应被视为鉴别诊断之一。