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类固醇治疗改善橄榄体肥大:两例具有独特表现的病例报告。

Olivary hypertrophy improved by steroid treatment: Two case reports with unique presentations.

机构信息

Department of Neurology and Neurological Science, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University, Japan.

Department of Diagnostic Radiology and Nuclear Medicine, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University, Japan.

出版信息

J Neuroimmunol. 2019 Sep 15;334:577003. doi: 10.1016/j.jneuroim.2019.577003. Epub 2019 Jul 5.

Abstract

Olivary hypertrophy (OH) is the secondary degeneration of the inferior olivary nucleus (ION). It is observed one month after the onset of a primary lesion within the dento-rubro-olivary pathway and is usually associated with oculopalatal tremors. Here, we report two unique cases with rare autoimmune diseases leading to OH development with progressive cerebellar ataxia, both of which improved with steroid treatment. The first patient was a 59-year-old man with slowly progressive dysarthria and ataxic gait without palatal tremor. Anti-N-methyl-d-aspartate (NMDA) receptor antibody was positive in the CSF, supporting a diagnosis of anti-NMDA receptor encephalitis. The second patient was a 56-year-old man who developed dysarthria, ataxia, gait disturbance, and palatal tremor. He was diagnosed with chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS), based on presence of a punctate contrast-enhancing lesion in the middle cerebellar peduncle, pons, and cerebellum on magnetic resonance imaging (MRI). Brain MRI in both patients demonstrated high signal intensity regions in the bilateral IONs. Semi-quantitative volume analysis of MRI revealed significant reduction in ION volume after steroid treatment and accordingly cerebellar ataxia was improved in both cases. Clinical and radiological features of the two cases were unique, indicating potential novel etiologies in the pathophysiology of OH associated with cerebellar ataxia.

摘要

橄榄体肥大(OH)是下橄榄核(ION)的继发性退化。它发生在齿状红橄榄束内的原发性病变出现后一个月,并通常与眼-腭-震颤有关。在这里,我们报告了两例伴有罕见自身免疫性疾病的独特病例,这些疾病导致 OH 发展并伴有进行性小脑共济失调,这两例均通过类固醇治疗得到改善。第一例患者为 59 岁男性,表现为进行性构音障碍和共济失调步态,无腭震颤。CSF 中的抗 N-甲基-D-天冬氨酸(NMDA)受体抗体阳性,支持抗 NMDA 受体脑炎的诊断。第二例患者为 56 岁男性,出现构音障碍、共济失调、步态障碍和腭震颤。基于磁共振成像(MRI)中桥脑、中脑和小脑存在点状对比增强病变,他被诊断为慢性淋巴细胞性炎症伴桥脑血管周围强化对类固醇反应良好(CLIPPERS)。两名患者的脑 MRI 均显示双侧 ION 高信号强度区域。MRI 的半定量体积分析显示类固醇治疗后 ION 体积明显减少,因此两例患者的小脑共济失调均得到改善。这两个病例的临床和影像学特征是独特的,表明与小脑共济失调相关的 OH 的病理生理学中存在潜在的新病因。

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