Neurobrucellosis

Rohit Sharma, Alice G. Willison
{"title":"Neurobrucellosis","authors":"Rohit Sharma, Alice G. Willison","doi":"10.1002/9781119467748.ch39","DOIUrl":null,"url":null,"abstract":"In 5-10% of cases of brucellosis may lead to central nervous system manifestation presenting most often as a meningitis or meningoencephalitis. We report three neurobrucellosis who have different presentation. First patient; a 49-year-old-woman who developed diffuse cerebral white matter lesions as leukoencephalopathy associated with neurobrucellosis, presented with gait disturbance, behavior change and seizure. Second patient; 44-year-old man was admitted to our hospital with a complaint of progressive motor weakness in his bilateral legs for four months and headache for one year. The patient’s symptoms may be explained with myeloradiculopathy and meningoencephalitis but the clinical picture didn’t correlate with imaging findings. Third patient; 23-year-old man was admitted to our hospital with a complaint of transient numbness attacks in his left of face and hand and headache for twenty days. He presented as meningitis which is the most clinical presentation of neurobrucellosis and meningovascular complications. Conclusively, brucellosis is still endemic in Turkey and thus neurobrucellosis should be considered in the unexplained neurological symptoms such as cognitive dysfunction, young transient ischemic attacks, paraparesis and psychiatric symptoms.","PeriodicalId":142057,"journal":{"name":"Infections of the Central Nervous System","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infections of the Central Nervous System","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/9781119467748.ch39","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

In 5-10% of cases of brucellosis may lead to central nervous system manifestation presenting most often as a meningitis or meningoencephalitis. We report three neurobrucellosis who have different presentation. First patient; a 49-year-old-woman who developed diffuse cerebral white matter lesions as leukoencephalopathy associated with neurobrucellosis, presented with gait disturbance, behavior change and seizure. Second patient; 44-year-old man was admitted to our hospital with a complaint of progressive motor weakness in his bilateral legs for four months and headache for one year. The patient’s symptoms may be explained with myeloradiculopathy and meningoencephalitis but the clinical picture didn’t correlate with imaging findings. Third patient; 23-year-old man was admitted to our hospital with a complaint of transient numbness attacks in his left of face and hand and headache for twenty days. He presented as meningitis which is the most clinical presentation of neurobrucellosis and meningovascular complications. Conclusively, brucellosis is still endemic in Turkey and thus neurobrucellosis should be considered in the unexplained neurological symptoms such as cognitive dysfunction, young transient ischemic attacks, paraparesis and psychiatric symptoms.
Neurobrucellosis
在5-10%的布鲁氏菌病病例中,可导致中枢神经系统表现,最常表现为脑膜炎或脑膜脑炎。我们报告三个神经布鲁氏菌病谁有不同的表现。第一个病人;一名49岁女性,出现弥漫性脑白质病变,表现为伴有神经布鲁氏菌病的脑白质病,表现为步态障碍、行为改变和癫痫发作。第二个病人;44岁男性因进行性双侧下肢运动无力4个月及头痛1年而入院。患者的症状可能与脊髓根病和脑膜脑炎有关,但临床表现与影像学表现不一致。第三个病人;男,23岁,主诉左脸、手一过性麻木发作,头痛20天。他表现为脑膜炎,这是神经布鲁氏菌病和脑膜血管并发症最常见的临床表现。最后,布鲁氏菌病在土耳其仍是地方性疾病,因此神经布鲁氏菌病应被认为是无法解释的神经系统症状,如认知功能障碍、青年短暂性脑缺血发作、麻痹和精神症状。
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:481959085
Book学术官方微信