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Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report

机译:肌萎缩性侧索硬化症和多发性硬化症重叠:一例报告

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The concurrence of amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS) is extremely rare. We reported the case of a 33-year-old woman with a past history of paresthesias at the right hand, who developed progressive quadriparesis with muscular atrophy of limbs and, finally, bulbar signs and dyspnea. Clinical and neurophysiologic investigations revealed upper and lower motor neuron signs in the bulbar region and extremities, suggesting the diagnosis of ALS. Moreover, magnetic resonance imaging (MRI) and cerebrospinal fluid (CSF) analysis demonstrated 3 periventricular and juxtacortical lesions, hyperintense in T2 and FLAIR sequences, and 3 liquoral immunoglobulin G (IgG) oligoclonal bands, consistent with diagnosis of primary progressive MS (PPMS). This unusual overlap of ALS and MS leads to the discussion of a hypothetical common pathological process of immunological dysfunction in these two disorders, although the role of immune response in ALS remains ambivalent and unclear.
机译:肌萎缩性侧索硬化症(ALS)和多发性硬化症(MS)的并发非常罕见。我们报道了一名33岁的女性,右手有感觉异常的病史,该妇女发展为进行性四肢瘫痪伴四肢肌肉萎缩,最后出现延髓症状和呼吸困难。临床和神经生理学调查显示,在延髓区和四肢上和下运动神经元体征,提示ALS的诊断。此外,磁共振成像(MRI)和脑脊液(CSF)分析显示3个心室和皮层皮损,T2和FLAIR序列中的高强度以及3个酒类免疫球蛋白G(IgG)寡克隆条带,与原发性进行性MS(PPMS)的诊断一致。 ALS和MS的这种异常重叠导致讨论了这两种疾病中免疫功能异常的假设性常见病理过程的讨论,尽管ALS中免疫反应的作用仍然不清楚且不清楚。

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