CNS B cell infiltration in tumefactive anti-myelin oligodendrocyte glycoprotein antibody-associated disease.

IF 2.5 Q2 CLINICAL NEUROLOGY
Ryotaro Ikeguchi, Natsuki Kanda, Masaki Kobayashi, Kenta Masui, Masayuki Nitta, Tatsuro Misu, Yoshihiro Muragaki, Takakazu Kawamata, Noriyuki Shibata, Kazuo Kitagawa, Yuko Shimizu
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引用次数: 0

Abstract

Background: Few studies have examined B cells among patients with anti-myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD), including brain pathology.

Objective: To describe cases of tumefactive MOGAD with B-cell dominant central nervous system (CNS) infiltration.

Methods: In this study, we reviewed three cases with clinical and brain histopathological features with tumefactive MOGAD.

Results: Forty-nine cases of tumefactive brain lesions (TBL) between January 2003 and December 2023 were included; of these, seven had MOGAD. Three underwent a brain biopsy. B-cell dominant CNS infiltration was observed in two cases. In two cases with B-cell dominant CNS infiltration, symptoms included fever, headache, nausea, somnolence, and focal neurological deficits. Cerebrospinal fluid examination revealed both mild pleocytosis and negative oligoclonal IgG bands. Magnetic resonance imaging of the brain revealed large abnormal lesions extending from the basal ganglia to the parietotemporal lobe in both cases. These cases showed a good response to steroids; however, one case relapsed. Brain pathology showed demyelination and perivascular lymphocytic infiltration. One showed small vessel vasculitis. Deposition of the activated complement component was absent or rarely observed. Loss of MOG was observed in two cases.

Conclusion: MOGAD could exhibit B-cell dominant CNS infiltration and small vessel vasculitis. MOGAD should be considered in differential diagnosis of TBL.

肿瘤性抗髓鞘少突胶质细胞糖蛋白抗体相关疾病的中枢神经系统B细胞浸润。
背景:很少有研究检测抗髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病(MOGAD)患者的B细胞,包括脑部病理。目的:探讨伴有b细胞显性中枢神经系统浸润的肿瘤性MOGAD病例。方法:回顾性分析3例具有肿瘤性MOGAD临床及脑组织病理学特征的病例。结果:2003年1月至2023年12月共纳入49例脑肿瘤;其中7个有MOGAD。其中三人接受了脑部活检。2例中枢神经系统可见b细胞显性浸润。在2例以b细胞为主的中枢神经系统浸润病例中,症状包括发热、头痛、恶心、嗜睡和局灶性神经功能缺损。脑脊液检查显示轻度多胞症和寡克隆IgG阴性。脑磁共振成像显示,两例患者均有从基底节区延伸至顶颞叶的巨大异常病变。这些病例对类固醇反应良好;然而,1例复发。脑病理表现为脱髓鞘及血管周围淋巴细胞浸润。一例为小血管炎。活化补体成分的沉积不存在或很少观察到。2例观察到MOG缺失。结论:MOGAD可表现为b细胞显性中枢神经浸润和小血管炎。在TBL的鉴别诊断中应考虑MOGAD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
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