Gorgel, AhmetTecellioğlu, MehmetÇankaya, Cem2021-12-292021-12-292019GÖRGEL A,TECELLİOĞLU M,ÇANKAYA C (2019). Autoimmune polyglandular syndrome type III which accompanies to multiple sclerosis: A case report. Annals of Medical Research, 26(12), 3053 - 3057. Doi: 10.5455/annalsmedres.2019.07.4202636-7688https://doi.org/10.5455/annalsmedres.2019.07.420https://hdl.handle.net/11616/44605https://search.trdizin.gov.tr/yayin/detay/359381Abstract: Autoimmune polyglandular syndrome type III (APS III) is characterised by autoimmune destruction of various endocrine and nonendocrine tissues. It differs from APS I and APS II in terms of without adrenal involvement. Although APS III includes a series ofautoimmune disorders, it is rarely associated with multiple sclerosis (MS). A 41-year-old female patient had diplopia, visual blurring,dizziness, and giddiness for 2 weeks. In her medical history, she had a diagnosis of MS and using Teriflunomide. It was detectedpositivity of antinuclear antibody (ANA), anti-thyroid peroxidase (Anti-TPO) and anti-thyroglobulin (Anti-TG) antibodies. Based onthese results, the patient with MS who has chronic autoimmune thyroiditis and primary ovarian failure was diagnosed with APSIII. The coexistence of APS-III and MS is a rare clinical entity. Moreover, hypothyroidism has been detected during teriflunomidetherapy in the patient. Hypothyroidism was most likely a component of APS-III in our case, but it may also have been triggered byteriflunomide.eninfo:eu-repo/semantics/openAccessAutoimmune polyglandular syndrome type III which accompanies to multiple sclerosis: A case reportArticle26123053305710.5455/annalsmedres.2019.07.420359381