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急性小脑表现而无边缘系统累及的 GABA 受体自身免疫性脑炎:病例报告及文献复习。

Acute Cerebellar Manifestations without Limbic Involvement in GABA Receptor Autoimmune Encephalitis: Case Report and Literature Review.

机构信息

Department of Neurology, Showa University Fujigaoka Hospital, 1-30 Fujigaoka Aoba-ku, Yokohama, 227-8501, Kanagawa, Japan.

出版信息

Cerebellum. 2024 Dec;23(6):2650-2654. doi: 10.1007/s12311-024-01729-3. Epub 2024 Aug 13.

Abstract

Autoimmune encephalitis is a rapidly progressive inflammatory brain disease. Gamma-aminobutyric acid type B (GABA) receptor autoimmune encephalitis is a rare subtype characterized by distinct clinical features. Diagnosis can be especially challenging when typical limbic symptoms and neuroimaging findings are absent. This case report underscores the importance of identifying this condition and starting immunosuppressive treatment promptly. A 59-year-old man presented with gait disturbances, dysarthria, and severe ataxia without cognitive impairment. Initial examinations, including a brain MRI, were unremarkable, except for an elevated cell count and protein in the cerebrospinal fluid. Despite receiving initial empirical antiviral treatment, his symptoms worsened, prompting the administration of intravenous methylprednisolone and immunoglobulin. After these immunosuppressive therapies, the cerebellar symptoms showed gradual improvement. Subsequent testing for antibodies to the GABA receptor was positive in both the serum and cerebrospinal fluid. Follow-up MRI revealed cerebellar atrophy, consistent with a diagnosis of GABA receptor-associated acute cerebellitis. This case illustrates that cerebellar symptoms can occur in the absence of more common limbic manifestations in GABA receptor autoimmune encephalitis. The progression of cerebellar atrophy following an initially normal MRI is a significant finding that offers supporting evidence for the diagnosis of cerebellitis. A review of the literature identified similar cases of acute cerebellitis without limbic symptoms, although neuroimaging abnormalities in the cerebellum were not reported. Our case underscores the importance of increased clinical awareness and consideration of autoimmune causes, even when neuroimaging appears normal. Early and appropriate immunosuppressive therapy may help change the course of the disease and enhance patient outcomes.

摘要

自身免疫性脑炎是一种快速进展的炎症性脑疾病。γ-氨基丁酸 B 型(GABA)受体自身免疫性脑炎是一种罕见亚型,具有独特的临床特征。当典型的边缘系统症状和神经影像学发现缺失时,诊断尤其具有挑战性。本病例报告强调了识别这种情况并及时开始免疫抑制治疗的重要性。一名 59 岁男性因步态障碍、构音障碍和严重共济失调而就诊,无认知障碍。初始检查,包括脑部 MRI,均无明显异常,除脑脊液细胞计数和蛋白升高外。尽管接受了初始经验性抗病毒治疗,但他的症状恶化,促使给予静脉甲基强的松龙和免疫球蛋白。在这些免疫抑制治疗后,小脑症状逐渐改善。随后对 GABA 受体抗体的检测在血清和脑脊液中均为阳性。随访 MRI 显示小脑萎缩,符合 GABA 受体相关急性小脑炎的诊断。本病例说明,在 GABA 受体自身免疫性脑炎中,小脑症状可在无更常见的边缘系统表现的情况下出现。小脑萎缩在最初正常 MRI 后进展是一个重要发现,为小脑炎的诊断提供了支持证据。文献复习发现了类似的无边缘系统症状的急性小脑炎病例,但未报告小脑的神经影像学异常。我们的病例强调了提高临床意识并考虑自身免疫原因的重要性,即使神经影像学正常也是如此。早期和适当的免疫抑制治疗可能有助于改变疾病进程并改善患者预后。

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