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一名患有川崎病的婴儿:病例报告及文献综述

An Infant With Kawasaki Disease: A Case Report and Literature Review.

作者信息

Ren Yifan

机构信息

Department of Paediatrics, Shaoxing Keqiao Women and Children's Hospital, Shaoxing, CHN.

出版信息

Cureus. 2024 Jul 23;16(7):e65221. doi: 10.7759/cureus.65221. eCollection 2024 Jul.

DOI:10.7759/cureus.65221
PMID:39184731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11343483/
Abstract

Kawasaki disease (KD) is the leading cause of acquired heart disease in children in developed countries. Delayed treatment can lead to coronary artery (CA) abnormalities, potentially causing myocardial ischemia, infarction, and death. Younger age is a risk factor for developing bilateral large CA aneurysms in KD patients. A one-and-a-half-month-old infant presented with fever and elevated inflammatory markers. Post-admission ceftriaxone injections were ineffective. Subsequently, the patient experienced recurrent high fevers, accompanied by rashes, erythema, and induration of the palms and soles, erythema, swelling at the Bacillus Calmette-Guerin (BCG) scar site, cracked lips, and conjunctival hyperemia, all of which were indicative of KD. Intravenous immunoglobulin (IVIG) and aspirin were administered on the third day of fever. Follow-ups at one, three, six, and 12 months post discharge revealed normal findings. This case demonstrates that even very young infants can develop complete KD, and early treatment can prevent CA complications.

摘要

川崎病(KD)是发达国家儿童后天性心脏病的主要病因。治疗延迟可导致冠状动脉(CA)异常,可能引起心肌缺血、梗死和死亡。年龄较小是KD患者发生双侧大型CA动脉瘤的危险因素。一名1个半月大的婴儿出现发热和炎症标志物升高。入院后注射头孢曲松无效。随后,患者反复高热,伴有皮疹、红斑、手掌和足底硬结、卡介苗(BCG)瘢痕部位红斑、肿胀、嘴唇干裂和结膜充血,所有这些均提示KD。发热第三天给予静脉注射免疫球蛋白(IVIG)和阿司匹林。出院后1个月、3个月、6个月和12个月的随访结果均正常。该病例表明,即使是非常小的婴儿也可能患完全性KD,早期治疗可预防CA并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/cd9ea7b96e61/cureus-0016-00000065221-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/2aa04a13089b/cureus-0016-00000065221-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/decb4c8012d2/cureus-0016-00000065221-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/cd9ea7b96e61/cureus-0016-00000065221-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/2aa04a13089b/cureus-0016-00000065221-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/decb4c8012d2/cureus-0016-00000065221-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7445/11343483/cd9ea7b96e61/cureus-0016-00000065221-i03.jpg

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本文引用的文献

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Retropharyngeal abscess-like as an atypical presentation of Kawasaki disease: a case report and literature review.咽后脓肿样表现的川崎病:一例病例报告并文献复习。
Pediatr Rheumatol Online J. 2023 Apr 13;21(1):34. doi: 10.1186/s12969-023-00812-z.
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An atypical case of Kawasaki disease with severe pneumonia in a neonate.一例新生儿川崎病合并重症肺炎的不典型病例。
BMC Pediatr. 2022 Mar 14;22(1):132. doi: 10.1186/s12887-022-03203-7.
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Giant bilateral axillary artery aneurysms with left complete obstructive thrombus in intravenous immunoglobulin-sensitive Kawasaki disease: a case report.
静脉注射免疫球蛋白敏感型川崎病致巨大双侧腋动脉动脉瘤伴左侧完全性血栓形成:病例报告。
Pediatr Rheumatol Online J. 2021 Nov 8;19(1):157. doi: 10.1186/s12969-021-00643-w.
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Multisystem inflammatory syndrome in children and Kawasaki disease: a critical comparison.儿童多系统炎症综合征与川崎病:关键对比。
Nat Rev Rheumatol. 2021 Dec;17(12):731-748. doi: 10.1038/s41584-021-00709-9. Epub 2021 Oct 29.
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Kawasaki disease without fever: A rare case in a 3-month old.无发热的川崎病:一名3个月大婴儿的罕见病例。
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SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?SARS-CoV-2 相关 MIS-C:川崎病病毒和遗传病因的关键?
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A 10-year cross-sectional retrospective study on Kawasaki disease in Iranian children: incidence, clinical manifestations, complications, and treatment patterns.一项关于伊朗儿童川崎病的 10 年回顾性横断面研究:发病率、临床表现、并发症和治疗模式。
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Kawasaki-like disease in children with COVID-19: A hypothesis.儿童 COVID-19 相关川崎样疾病:一种假说。
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Epidemiology, Treatments, and Cardiac Complications in Patients with Kawasaki Disease: The Nationwide Survey in Japan, 2017-2018.2017-2018 年日本全国川崎病患者的流行病学、治疗方法和心脏并发症调查。
J Pediatr. 2020 Oct;225:23-29.e2. doi: 10.1016/j.jpeds.2020.05.034. Epub 2020 May 23.
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