川崎病合并冠状动脉动脉瘤的不典型表现在一个2.5个月大的婴儿:一个来自叙利亚的病例报告。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Clinical Medicine Insights. Case Reports Pub Date : 2025-08-05 eCollection Date: 2025-01-01 DOI:10.1177/11795476251359774
Suzan Mahfoud, Aous Arous, Danial Antonios, Hussein Jasser, Abdulrahman Shbani
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引用次数: 0

摘要

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。本报告描述了一个2.5个月大的婴儿出现持续15天发烧的病例,最初被误认为是咽炎和中耳炎。实验室检查显示明显的白细胞增多、血小板增多和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,证实了KD的诊断。婴儿接受静脉注射免疫球蛋白(IVIG)和大剂量阿司匹林,发热消退。症状复发需要额外的IVIG和皮质类固醇治疗。随后的影像学显示持续的冠状动脉扩张,强调了持续血管并发症的风险。这个病例强调了诊断婴儿KD的挑战,特别是那些不典型的表现。及时诊断和治疗对于预防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患有长期不明原因发热的婴儿的KD,以改善预后并将心脏相关风险降至最低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

Atypical Presentation of Kawasaki Disease With Coronary Artery Aneurysms in a 2.5-Month-Old Infant: A Case Report From Syria.

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.

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来源期刊
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights. Case Reports MEDICINE, GENERAL & INTERNAL-
CiteScore
1.10
自引率
0.00%
发文量
57
审稿时长
8 weeks
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