Lymphomatosis cerebri with coexistent anti-N-methyl-D-aspartate receptor antibody: A case report.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Neuropathology Pub Date : 2023-10-01 Epub Date: 2023-02-22 DOI:10.1111/neup.12899
Natthapon Rattanathamsakul, Tatchaporn Ongphichetmetha, Pattharasaya Weerachotisakul, Nanthaya Tisavipat, Pornsuk Cheunsuchon, Jiraporn Jitprapaikulsan
{"title":"Lymphomatosis cerebri with coexistent anti-N-methyl-D-aspartate receptor antibody: A case report.","authors":"Natthapon Rattanathamsakul,&nbsp;Tatchaporn Ongphichetmetha,&nbsp;Pattharasaya Weerachotisakul,&nbsp;Nanthaya Tisavipat,&nbsp;Pornsuk Cheunsuchon,&nbsp;Jiraporn Jitprapaikulsan","doi":"10.1111/neup.12899","DOIUrl":null,"url":null,"abstract":"<p><p>Diagnosis of lymphomatosis cerebri (LC) is usually delayed because of its rarity and the need for pathological confirmation. The association of LC with humoral immunity has scarcely been reported. Herein, we present a woman with a 2-week history of dizziness and gait ataxia, followed by diplopia, altered mental status, and spasticity of all limbs. Magnetic resonance imaging (MRI) of the brain showed multifocal lesions involving bilateral subcortical white matter, deep gray structures, and brainstem. Oligoclonal bands and anti-N-methyl-D-aspartate receptor (NMDAR) antibodies were present in cerebrospinal fluid (CSF) twice. She was initially treated with methylprednisolone but still worsening. A stereotactic brain biopsy confirmed the diagnosis of LC. This is a report on the distinctive coexistence of the rare CNS lymphoma variant and the anti-NMDAR antibody.</p>","PeriodicalId":19204,"journal":{"name":"Neuropathology","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuropathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/neup.12899","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/2/22 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Diagnosis of lymphomatosis cerebri (LC) is usually delayed because of its rarity and the need for pathological confirmation. The association of LC with humoral immunity has scarcely been reported. Herein, we present a woman with a 2-week history of dizziness and gait ataxia, followed by diplopia, altered mental status, and spasticity of all limbs. Magnetic resonance imaging (MRI) of the brain showed multifocal lesions involving bilateral subcortical white matter, deep gray structures, and brainstem. Oligoclonal bands and anti-N-methyl-D-aspartate receptor (NMDAR) antibodies were present in cerebrospinal fluid (CSF) twice. She was initially treated with methylprednisolone but still worsening. A stereotactic brain biopsy confirmed the diagnosis of LC. This is a report on the distinctive coexistence of the rare CNS lymphoma variant and the anti-NMDAR antibody.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
同时存在抗N-甲基-D-天冬氨酸受体抗体的脑淋巴瘤1例报告。
大脑淋巴瘤病(LC)的诊断通常因其罕见性和需要病理证实而延迟。LC与体液免疫的关系几乎没有报道。在此,我们介绍了一位有两周头晕和步态共济失调病史的女性,随后出现复视、精神状态改变和四肢痉挛。大脑磁共振成像(MRI)显示多灶性病变,涉及双侧皮质下白质、深灰色结构和脑干。脑脊液中出现两次寡克隆带和抗N-甲基-D-天冬氨酸受体(NMDAR)抗体。她最初接受了甲基强的松龙治疗,但病情仍在恶化。立体定向脑活检证实了LC的诊断。这是一份关于罕见中枢神经系统淋巴瘤变体和抗NMDAR抗体独特共存的报告。
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 去求助
来源期刊
Neuropathology
Neuropathology 医学-病理学
CiteScore
4.10
自引率
4.30%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Neuropathology is an international journal sponsored by the Japanese Society of Neuropathology and publishes peer-reviewed original papers dealing with all aspects of human and experimental neuropathology and related fields of research. The Journal aims to promote the international exchange of results and encourages authors from all countries to submit papers in the following categories: Original Articles, Case Reports, Short Communications, Occasional Reviews, Editorials and Letters to the Editor. All articles are peer-reviewed by at least two researchers expert in the field of the submitted paper.
期刊最新文献
Primary intracranial dedifferentiated liposarcoma: An extremely rare site with unusual histopathological findings. Solitary subependymal giant cell astrocytoma lacking TSC1/2 mutations and TTF-1 expression: A potential diagnostic pitfall. Adenoid glioblastoma: Stromal hypovascularity and secretion of chondromodulin-I by tumor cells. Pathological study of progressive supranuclear palsy the cases with mutations in Bassoon. Anti-neutrophil cytoplasmic antibody-associated central nervous system vasculitis mimicking brain tumor: A case report.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1