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麸质共济失调和 mGluR1 自身免疫性脑炎表现为急性小脑共济失调:病例报告。

Gluten Ataxia and mGluR1 Autoimmune Encephalitis Presenting as Acute Cerebellar Ataxia: A Case Report.

机构信息

University of South Dakota Sanford School of Medicine.

Sanford USD Medical Center, Sioux Falls, South Dakota.

出版信息

S D Med. 2024 May;77(5):207-210.

Abstract

A Caucasian male in his 60s presented with acute onset of dizziness, dysarthria, and gait ataxia. Upon extensive workup, positive findings were cerebrospinal fluid (CSF) showing lymphocytic pleocytosis with oligoclonal bands, positive celiac disease autoantibodies in blood, a duodenal biopsy indicating lymphocytic infiltration, and positive anti-mGluR1 antibody titers in CSF. The patient was started on a strict gluten-free diet and intravenous immunoglobulin therapy for 5 days and showed mild consecutive improvements each day of treatment. He was discharged after 22 days, and was encouraged to continue gluten adherence, physical and speech therapy, and follow up with neuroimmunology. This report demonstrates that autoimmune encephalitis due to anti-mGluR1antibodies and gluten ataxia are both immune-mediated disorders that should be considered in acute cerebellar ataxia cases. By broadening the differential diagnosis and a comprehensive CSF analysis, identification of gluten ataxia and autoimmune encephalitis were beneficial in the management of this particular patient.

摘要

一位 60 多岁的高加索男性出现急性头晕、构音障碍和步态共济失调。经过广泛的检查,发现脑脊液(CSF)中有淋巴细胞增多症伴寡克隆带,血液中有阳性乳糜泻自身抗体,十二指肠活检显示淋巴细胞浸润,CSF 中有阳性抗 mGluR1 抗体滴度。患者开始接受严格的无麸质饮食和静脉注射免疫球蛋白治疗 5 天,治疗期间每天都有轻微的连续改善。他在 22 天后出院,并被鼓励继续坚持无麸质饮食、进行物理和言语治疗,并接受神经免疫学随访。本报告表明,抗 mGluR1 抗体和麸质共济失调引起的自身免疫性脑炎均为免疫介导的疾病,在急性小脑共济失调病例中应考虑这两种疾病。通过扩大鉴别诊断和全面的 CSF 分析,确定麸质共济失调和自身免疫性脑炎有助于管理该特定患者。

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