054 An adult case of acute cerebellitis as a manifestation of Mycoplasma Pneumoniae infection

A. Ji, Michael Roizman, Andrew Swayne
{"title":"054 An adult case of acute cerebellitis as a manifestation of Mycoplasma Pneumoniae infection","authors":"A. Ji, Michael Roizman, Andrew Swayne","doi":"10.1136/bmjno-2021-anzan.54","DOIUrl":null,"url":null,"abstract":"Introduction Acute cerebellitis is exceptionally rare in adults often preceded by systemic viral or bacterial infections. We present a case of acute cerebellitis following otherwise asymptomatic Mycoplasma Pneumoniae infection. Case Descriptions A 40-year-old man presented with a three-day history of acute onset of dizziness, vomiting and headache which was initially diagnosed and managed as vestibular neuritis. He was discharged and four days later represented with slurred speech and difficulty walking. On examination, he was alert, had an ataxic gait, dysarthria and bilateral hypermetric saccades. CSF studies showed an elevated leukocyte count of 152X106/L with 100% mononuclear cells and a mildly elevated protein level of 0.7g/L with normal glucose. Other CSF analysis including a multiplex PCR panel for a variety of viral, bacterial and fungal pathogens, cytology, flow cytometry, antineuronal and encephalitis antibody tests were negative. MRI showed features consistent with acute cerebellitis including subtle diffuse cerebellar hyperintense signal on T2 and FLAIR sequences. Serological testing showed the presence of Mycoplasma Pneumoniae IgM and IgG. A diagnosis of acute cerebellitis was made, and the patient received supportive care and made a complete neurological recovery after 10 days. A repeat MRI one month later showed imaging resolution and he remained asymptomatic at clinic follow-up. Conclusion This case describes an adult with cerebellitis most likely secondary to Mycoplasma Pneumoniae infection with other causes excluded on extensive investigation. Although rare, acute cerebellitis should be considered as a part of the differential diagnosis of acute vertigo particularly in the presence of cerebellar signs.","PeriodicalId":20317,"journal":{"name":"Poster Discussion Abstracts","volume":"93 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poster Discussion Abstracts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/bmjno-2021-anzan.54","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

Introduction Acute cerebellitis is exceptionally rare in adults often preceded by systemic viral or bacterial infections. We present a case of acute cerebellitis following otherwise asymptomatic Mycoplasma Pneumoniae infection. Case Descriptions A 40-year-old man presented with a three-day history of acute onset of dizziness, vomiting and headache which was initially diagnosed and managed as vestibular neuritis. He was discharged and four days later represented with slurred speech and difficulty walking. On examination, he was alert, had an ataxic gait, dysarthria and bilateral hypermetric saccades. CSF studies showed an elevated leukocyte count of 152X106/L with 100% mononuclear cells and a mildly elevated protein level of 0.7g/L with normal glucose. Other CSF analysis including a multiplex PCR panel for a variety of viral, bacterial and fungal pathogens, cytology, flow cytometry, antineuronal and encephalitis antibody tests were negative. MRI showed features consistent with acute cerebellitis including subtle diffuse cerebellar hyperintense signal on T2 and FLAIR sequences. Serological testing showed the presence of Mycoplasma Pneumoniae IgM and IgG. A diagnosis of acute cerebellitis was made, and the patient received supportive care and made a complete neurological recovery after 10 days. A repeat MRI one month later showed imaging resolution and he remained asymptomatic at clinic follow-up. Conclusion This case describes an adult with cerebellitis most likely secondary to Mycoplasma Pneumoniae infection with other causes excluded on extensive investigation. Although rare, acute cerebellitis should be considered as a part of the differential diagnosis of acute vertigo particularly in the presence of cerebellar signs.
以肺炎支原体感染为表现的成人急性小脑炎1例
急性小脑炎在成人中是非常罕见的,通常在系统性病毒或细菌感染之前。我们报告一例急性小脑炎后,否则无症状肺炎支原体感染。病例描述一名40岁男性,有三天的急性头晕、呕吐和头痛病史,最初诊断和治疗为前庭神经炎。他出院了,四天后表现为言语不清,行走困难。检查时,他清醒,步态共济失调,构音障碍和双侧高速扫视。脑脊液研究显示100%单核细胞时白细胞计数升高152X106/L,正常葡萄糖时蛋白水平轻度升高0.7g/L。其他脑脊液分析包括多种病毒、细菌和真菌病原体的多重PCR检测、细胞学、流式细胞术、抗神经元和脑炎抗体检测均为阴性。MRI表现为急性小脑炎的特征,包括T2和FLAIR序列上细微的弥漫性小脑高信号。血清学检测显示存在肺炎支原体IgM和IgG。诊断为急性小脑炎,患者接受支持性治疗,10天后神经系统完全恢复。一个月后复查核磁共振成像显示成像清晰,临床随访时患者仍无症状。结论:本病例描述了一例成人小脑炎,很可能继发于肺炎支原体感染,经广泛调查排除了其他原因。尽管罕见,急性小脑炎应被视为急性眩晕鉴别诊断的一部分,特别是在小脑体征的存在。
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