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

BACKGROUND: Primary Sjögren 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 RESULT...

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Detalles Bibliográficos
Autores principales: Sun, Jia-Yue, Liu, Zheng, Zhao, Peng, Liu, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591106/
https://www.ncbi.nlm.nih.gov/pubmed/27858858
http://dx.doi.org/10.1097/MD.0000000000005194
Descripción
Sumario:BACKGROUND: Primary Sjögren 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.