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Sj?gren’s syndrome and Neuromyelitis Optica spectrum disorders (NMOSD) - a case report and review of literature

机译:干燥综合征和视神经脊髓炎光谱症(NMOSD)-病例报告和文献复习

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Background Neuromyelitis optica (NMO) is a rare relapsing auto-immune disease of the central nervous system which is sometimes found in association with other autoimmune disorders including Sjogren’s syndrome. We present the case of a middle aged female with Sjogren’s syndrome (SS) and Neuromyelitis optica spectrum disorders (NMOSD) who had a rapidly declining neurological illness that responded to immunosuppressive therapy. Case presentation A 51-year-old female with Sjogren’s syndrome and recent history of varicella zoster infection presented with right upper and lower extremity weakness of one week duration. She was noted to have contrast enhancement at C2-C4 cord levels on cervico-thoracic MRI. Comprehensive work up was negative except for presence of a mild lymphocytic pleocytosis and oligoclonal bands in the CSF. She was diagnosed with transverse myelitis secondary to varicella zoster infection and was treated with high dose steroids in addition to acyclovir with improvement in her symptoms. Two months later she developed left upper and lower extremity weakness, bilateral dysesthesias and urinary incontinence. Repeat MRI of the cervico-thoracic spine revealed worsening enhancement at lower cervical cord levels (C5-7) with extension to T1. CSF analysis was unchanged; however immunological work up was abnormal for elevated NMO-IgG/AQP4 antibody. She was diagnosed with NMOSD and was treated with immunosuppressive therapy. Initially with IV methylprednisone and Cyclophosphamide therapy followed by Mycophenolate mofetil (MMF) maintenance therapy with good response. Repeat MRI 6 months later showed near complete resolution of previous abnormal cord signal changes. Conclusion One needs to recognize the relationship between autoimmune diseases especially SS and NMOSD. The presence of NMO antibody has been associated with a relapsing disease course and a careful follow-up, besides use of remission maintenance agents such as MMF and Azathioprine are important to consider.
机译:背景技术视神经脊髓炎(NMO)是一种罕见的中枢神经系统复发性自身免疫性疾病,有时与其他自身免疫性疾病(包括干燥综合征)相关。我们介绍了一个患有干燥综合征(SS)和视神经脊髓炎谱系疾病(NMOSD)的中年女性,该病例的神经系统疾病迅速下降,对免疫抑制疗法有反应。病例介绍一位患有干燥综合征的51岁女性,近期有水痘带状疱疹感染史,右上肢和下肢无力,持续时间为一周。注意到她在颈胸MRI的C2-C4脐带水平具有对比增强作用。综合检查为阴性,除了在脑脊液中存在轻度淋巴细胞性细胞增多和寡克隆带。她被诊断出患有水痘带状疱疹感染继发的横性脊髓炎,除阿昔洛韦外还接受了大剂量类固醇的治疗,症状得到改善。两个月后,她出现左上肢和下肢无力,双侧感觉异常和尿失禁。子宫颈胸椎重复MRI显示,颈椎较低水平(C5-7)的增强作用随着T1的延长而恶化。脑脊液分析未改变;但是,NMO-IgG / AQP4抗体升高的免疫检查异常。她被诊断出患有NMOSD,并接受了免疫抑制治疗。最初采用静脉注射甲基泼尼松和环磷酰胺治疗,随后进行霉酚酸酯(MMF)维持治疗,反应良好。 6个月后重复MRI,显示以前的异常脐带信号变化几乎完全消失。结论必须认识到自身免疫性疾病特别是SS和NMOSD之间的关系。 NMO抗体的存在与疾病的复发有关,并且除了要考虑使用缓解维持剂(如MMF和硫唑嘌呤)外,还应进行仔细的随访。

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