儿童菊池-藤本病并发无菌性脑膜炎或脑炎:一项病例对照研究

IF 2 3区 医学 Q2 PEDIATRICS
Bing Liu, Yi Sun, Bing Hu, Wen-Yuan Shi, Tian-Ming Chen, Lin-Lin Liu, Gang Liu
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引用次数: 0

摘要

背景:本研究旨在总结合并无菌性脑膜炎或脑炎的菊池-藤本病患儿的临床和实验室特征。方法:对2015年1月至2023年12月在北京儿童医院诊断为菊池-藤本病的患儿进行病例对照研究,了解该疾病并发无菌性脑膜炎或脑炎的特点。结果:我们的队列64例菊池-藤本病包括16例中枢神经系统受累的儿童和48例对照。16例患儿中,男女比例为1.7:1.0。发病年龄3 ~ 13岁,中位年龄8岁。16例患者均有发热,15例颈淋巴结压痛,11例头痛,14例血常规白细胞计数下降。头部影像学显示11例异常,特别是脑白质病,主要累及双侧。颈部淋巴结压痛、头痛、意识不清、抽搐和c反应蛋白升高与合并无菌性脑膜炎或脑炎的Kikuchi-Fujimoto病显著相关(p结论:对于患有Kikuchi-Fujimoto病的儿童,当颈部淋巴结压痛、c反应蛋白升高或乳酸脱氢酶升高时,需要仔细评估中枢神经系统是否受累。在以无菌性脑膜炎或脑炎为表现的儿童中,应将菊池-藤本病作为鉴别诊断。临床试验号:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kikuchi-Fujimoto disease concurrent with aseptic meningitis or encephalitis in children: a case-control study.

Background: This study was performed to summarize the clinical and laboratory features of children with Kikuchi-Fujimoto disease concurrent with aseptic meningitis or encephalitis.

Methods: A case-control study of children diagnosed with Kikuchi-Fujimoto disease at Beijing Children's Hospital from January 2015 to December 2023 was conducted to determine the characteristics of the disease when concurrent with aseptic meningitis or encephalitis.

Results: Our cohort of 64 cases of Kikuchi-Fujimoto disease included 16 children with central nervous system involvement and 48 controls. Among the 16 affected children, the male: female ratio was 1.7:1.0. The age at onset ranged from 3 to 13 years, with a median age of 8 years. All 16 cases had fever, 15 had cervical lymph node tenderness, 11 had headache, and 14 showed decreased white blood cell counts in routine blood tests. Imaging of the head revealed abnormalities in 11 cases, specifically leukoencephalopathy with mostly bilateral involvement. Cervical lymph node tenderness, headache, confusion, convulsions, and elevated C-reactive protein were significantly associated with Kikuchi-Fujimoto disease concurrent with aseptic meningitis or encephalitis (p < 0.05). There was also a significant difference in lactate dehydrogenase levels between children with and without central nervous system involvement (575.8 ± 221.3 vs. 440.0 ± 163.1 U/L, p = 0.014).

Conclusions: For children with Kikuchi-Fujimoto disease, careful evaluation for central nervous system involvement is warranted when cervical lymph node tenderness, elevated C-reactive protein, or elevated lactate dehydrogenase is present. In children presenting with aseptic meningitis or encephalitis, Kikuchi-Fujimoto disease should be considered as a differential diagnosis.

Clinical trial number: Not applicable.

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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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