Boyraz, İsmailKoç, BünyaminYazıcı, Selma2021-06-232021-06-2320151309-02912148-5046https://doi.org/10.5606/ArchRheumatol.2015.5636https://hdl.handle.net/20.500.12491/8497https://app.trdizin.gov.tr/makale/TVRnNU5EQTJOZz09Sjogren’s syndrome (SS) is a systemic autoimmune disease that can involve both the peripheral nervous systems and central nervous systems (CNS). It is characterized by a lymphocytic infiltration of all exocrine glands.1 Neurologic symptoms including transverse myelitis, optic neuritis, stroke-like acute symptoms or several neurological disorders like progressive relapsing remitting attacks mimicking multiple sclerosis (MS) may develop in patients with SS. Herein, we reported a patient who had been treated/followed-up previously with the diagnosis of MS and was diagnosed subsequently with SS.eninfo:eu-repo/semantics/openAccessSjogren's SyndromeMultiple SclerosisCentral Nervous SystemLetter10.5606/ArchRheumatol.2015.56363043653662-s2.0-84949185174Q4TR-DizinIDWOS:000366027100015Q4