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Optic neuritis as an initial presentation of primary Sj?gren syndrome: A case report and literature review

机译:视神经炎是原发性干燥综合征的初步表现:一例病例报告并文献复习

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Background: Primary Sj?gren syndrome (pSS) is a progressive autoimmune disease that primarily affects exocrine glands. The clinical presentation of pSS may vary from an asymptomatic condition to severe skin symptom, resulting in a difficult and challenging diagnosis and treatment. Methods and results: Here, we report a 47-year-old Chinese woman who lost vision in the right eye for 7 days. She had been misdiagnosed with primary optic neuritis for 3 months. After 3 months, the results of immunohistochemistry, salivary gland scintigraphy, and antibody tests proved the diagnosis of pSS. After an IV methylprednisolone treatment for 3 days (1.0?g/d), her final visual and perimetry outcome were satisfactory. A review of the relevant English literature based on PubMed encompassing dates up to July 2016 has been discussed. Conclusion: Our finding and the literature review suggest that an early treatment may be beneficial but long-term disease may cause permanent irreparable damage.
机译:背景:原发性干燥综合征(pSS)是一种进行性自身免疫疾病,主要影响外分泌腺。 pSS的临床表现可能从无症状到严重的皮肤症状有所不同,导致诊断和治疗困难且具有挑战性。方法和结果:在这里,我们报道了一名47岁的中国妇女,右眼失明了7天。她被误诊为原发性视神经炎3个月。 3个月后,免疫组织化学,唾液腺闪烁显像和抗体检测的结果证明了pSS的诊断。静脉注射甲基强的松龙治疗3天(1.0?g / d)后,她的最终视觉和视野检查结果令人满意。讨论了基于PubMed的相关英语文献,涵盖截至2016年7月的日期。结论:我们的发现和文献综述表明,早期治疗可能是有益的,但长期疾病可能导致永久性不可修复的损害。

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