Mahfoud Suzan, Arous Aous, Antonios Danial, Jasser Hussein, Shbani Abdulrahman
Damascus University, Pediatrics Hospital, Tartous, Syria.
Faculty of Medicine, Tartous University, Syria.
Clin Med Insights Case Rep. 2025 Aug 5;18:11795476251359774. doi: 10.1177/11795476251359774. eCollection 2025.
Kawasaki disease (KD), a febrile vasculitis primarily affecting young children under 5, is commonly associated with coronary artery complications. This report describes the case of a 2.5-month-old infant presenting with a persistent 15-day fever, initially misidentified as pharyngitis and otitis media. Laboratory tests indicated significant leukocytosis, thrombocytosis, and increased C-reactive protein (CRP) levels. Echocardiography revealed coronary artery dilation and pericardial effusion, confirming a KD diagnosis. The infant received intravenous immunoglobulin (IVIG) and high-dose aspirin, which resolved the fever. Symptom recurrence necessitated additional IVIG and corticosteroid treatment. Subsequent imaging showed ongoing coronary dilation, emphasizing the risk of lasting vascular complications. This case underscores the diagnostic challenges of KD in infants, especially those with atypical presentations. Prompt diagnosis and treatment are critical to prevent serious complications such as coronary aneurysms. Healthcare providers should consider KD in infants with prolonged unexplained fevers to improve prognosis and minimize heart-related risks.
川崎病(KD)是一种主要影响5岁以下幼儿的发热性血管炎,通常与冠状动脉并发症有关。本报告描述了一名2.5个月大婴儿的病例,该婴儿持续发热15天,最初被误诊为咽炎和中耳炎。实验室检查显示白细胞显著增多、血小板增多以及C反应蛋白(CRP)水平升高。超声心动图显示冠状动脉扩张和心包积液,确诊为川崎病。该婴儿接受了静脉注射免疫球蛋白(IVIG)和高剂量阿司匹林治疗,发热症状得以缓解。症状复发需要额外的IVIG和皮质类固醇治疗。后续影像学检查显示冠状动脉持续扩张,凸显了持久血管并发症的风险。该病例强调了婴儿川崎病的诊断挑战,尤其是那些表现不典型的婴儿。及时诊断和治疗对于预防诸如冠状动脉瘤等严重并发症至关重要。医疗保健提供者应考虑对不明原因长期发热的婴儿进行川崎病排查,以改善预后并将心脏相关风险降至最低。