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神经型布鲁氏菌病酷似多发性硬化症:一例报告

Neurobrucellosis mimicking multiple sclerosis: a case report.

作者信息

Bussone G, La Mantia L, Grazzi L, Lamperti E, Salmaggi A, Strada L

机构信息

II Divisione di Neurologia, Istituto Neurologico C. Besta, Milano, Italia.

出版信息

Eur Neurol. 1989;29(4):238-40. doi: 10.1159/000116419.

DOI:10.1159/000116419
PMID:2474444
Abstract

A case of neurobrucellosis misdiagnosed at the onset as multiple sclerosis (MS) is presented. Magnetic resonance imaging showed multiple periventricular areas compatible with demyelinating lesions of possible vasculitic origin. Myelin basic protein was elevated in the CSF. The immunological CSF study was consistent with a chronic intrathecal inflammatory process. The modification of these parameters during specific treatment is also presented.

摘要

本文报告了一例最初被误诊为多发性硬化症(MS)的神经型布鲁氏菌病病例。磁共振成像显示多个脑室周围区域,与可能源于血管炎的脱髓鞘病变相符。脑脊液中髓鞘碱性蛋白升高。脑脊液免疫学研究结果与慢性鞘内炎症过程一致。文中还介绍了在特异性治疗过程中这些参数的变化情况。

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引用本文的文献

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Rev Soc Bras Med Trop. 2025 Sep 22;58:e01542025. doi: 10.1590/0037-8682-0154-2024. eCollection 2025.
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Case report of neurobrucellosis: a rare complication and neuroimaging findings of a common disease.神经型布鲁氏菌病病例报告:一种罕见并发症及常见疾病的神经影像学表现
Front Immunol. 2025 Jan 7;15:1449909. doi: 10.3389/fimmu.2024.1449909. eCollection 2024.
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From Pseudotumor Cerebri to Neurobrucellosis: A Journey With Several Lessons.
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Cureus. 2024 Apr 3;16(4):e57496. doi: 10.7759/cureus.57496. eCollection 2024 Apr.
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