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Acute motor-sensory axonal neuropathy associated with systemic lupus erythematosus

机译:与系统性红斑狼疮相关的急性运动感觉轴索神经病

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摘要

Systemic lupus erythematosus (SLE) is an autoimmune disease that involves multiple organs and is generally treated by immunosuppressive agents. Acute motor-sensory axonal neuropathy (AMSAN) is a variant of Guillain-Barré syndrome. The standard therapies are intravenous immunoglobulin or plasmapheresis. An association between AMSAN and SLE is rarely reported. Herein, we describe a case of a 72-year-old man who presented with rapidly progressive paraparesis, dysesthesia, and joint pain with morning stiffness. Initially, he was diagnosed with AMSAN. Intravenous immunoglobulin was given without significant improvement. Subsequent studies indicated the diagnosis of SLE. Therefore, the patient was treated with intravenous methylprednisolone, cyclophosphamide, and then plasmapheresis. At 3 months, he improved from bedridden to wheelchair-bound. Our case demonstrates AMSAN as a rare initial manifestation that can lead to significant disability.
机译:系统性红斑狼疮(SLE)是一种涉及多个器官的自身免疫性疾病,通常通过免疫抑制剂治疗。急性运动感觉轴索神经病(AMSAN)是格林-巴利综合征的一种变体。标准疗法是静脉内免疫球蛋白或血浆置换。很少报道AMSAN与SLE之间的关联。在此,我们描述了一个72岁的男性患者,该患者呈现出快速进行性轻瘫,感觉异常和关节僵硬并伴有早晨僵硬。最初,他被诊断出患有AMSAN。给予静脉免疫球蛋白无明显改善。随后的研究表明SLE的诊断。因此,该患者先后接受了静脉注射甲基强的松龙,环磷酰胺和血浆置换的治疗。在三个月的时间里,他从卧床不起变为坐轮椅。我们的案例表明,AMSAN是一种罕见的初始表现,可导致严重的残疾。

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