Multiple Sclerosis First Presentation in a Child: Diffuse Motor Demyelinating Polyradiculopathy: Case Report

W. Elnaggar, M. Kotb
{"title":"Multiple Sclerosis First Presentation in a Child: Diffuse Motor Demyelinating Polyradiculopathy: Case Report","authors":"W. Elnaggar, M. Kotb","doi":"10.21608/cupsj.2024.295970.1132","DOIUrl":null,"url":null,"abstract":": Multiple sclerosis is a mostly debilitating chronic demyelinating immune disease of the central nervous system that compromises quality of life within 10-15 years of onset. The clinical picture spectrum varies widely depending on the underlying pathogenesis of demyelination; the macrophage induced demyelination, antibody mediated against myelin proteins, T cell-mediated small vessel vasculitis and subsequent ischemia or cytokine mediated oligodendrocyte death. Axonal injury is limited to 5% of cases. Peripheral nerve demyelination is an exceptionally rare association of multiple sclerosis. We report a 9-year-old who developed bilateral lower limb weakness and loss of truncal support. Electromyography revealed demyelinating diffuse motor polyradiculopathy. He was diagnosed as Guillain-Barré syndrome and received intravenous immunoglobulins with no response. Magnetic resonance imaging of the brain and cervical spine revealed multiple cerebral and cerebellar foci of abnormal signal representing demyelination. He was diagnosed as multiple sclerosis and had a full recovery within 3 weeks from start of management by methylprednisolone. Peripheral demyelinating neuropathy may be the initial presentation of multiple sclerosis in a child.","PeriodicalId":153483,"journal":{"name":"Pediatric Sciences Journal","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Sciences Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/cupsj.2024.295970.1132","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

: Multiple sclerosis is a mostly debilitating chronic demyelinating immune disease of the central nervous system that compromises quality of life within 10-15 years of onset. The clinical picture spectrum varies widely depending on the underlying pathogenesis of demyelination; the macrophage induced demyelination, antibody mediated against myelin proteins, T cell-mediated small vessel vasculitis and subsequent ischemia or cytokine mediated oligodendrocyte death. Axonal injury is limited to 5% of cases. Peripheral nerve demyelination is an exceptionally rare association of multiple sclerosis. We report a 9-year-old who developed bilateral lower limb weakness and loss of truncal support. Electromyography revealed demyelinating diffuse motor polyradiculopathy. He was diagnosed as Guillain-Barré syndrome and received intravenous immunoglobulins with no response. Magnetic resonance imaging of the brain and cervical spine revealed multiple cerebral and cerebellar foci of abnormal signal representing demyelination. He was diagnosed as multiple sclerosis and had a full recovery within 3 weeks from start of management by methylprednisolone. Peripheral demyelinating neuropathy may be the initial presentation of multiple sclerosis in a child.
儿童首次出现多发性硬化症:弥漫性运动性脱髓鞘多发性硬化症:病例报告
:多发性硬化症是一种使人衰弱的慢性中枢神经系统脱髓鞘免疫性疾病,发病后 10-15 年内会影响患者的生活质量。根据脱髓鞘的潜在发病机制不同,临床表现也大相径庭:巨噬细胞诱导的脱髓鞘、抗体介导的髓鞘蛋白、T 细胞介导的小血管炎以及随后的缺血或细胞因子介导的少突胶质细胞死亡。轴突损伤仅限于 5%的病例。周围神经脱髓鞘是多发性硬化症的一种罕见并发症。我们报告了一名出现双下肢无力和失去躯干支撑力的 9 岁儿童。肌电图显示他患有脱髓鞘性弥漫性运动性多发性神经病。他被诊断为吉兰-巴雷综合征,接受了静脉注射免疫球蛋白,但没有任何反应。大脑和颈椎的磁共振成像显示多个大脑和小脑异常信号灶,代表脱髓鞘。他被诊断为多发性硬化症,并在开始使用甲泼尼龙治疗的 3 周内完全康复。周围脱髓鞘性神经病可能是儿童多发性硬化症的最初表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信