Autoimmune polyglandular syndrome type III which accompanies to multiple sclerosis: A case report
dc.contributor.author | Gorgel, Ahmet | |
dc.contributor.author | Tecellioglu, Mehmet | |
dc.contributor.author | Cankaya, Cem | |
dc.date.accessioned | 2022-03-08T09:49:57Z | |
dc.date.available | 2022-03-08T09:49:57Z | |
dc.date.issued | 2019 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | 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 of autoimmune 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 detected positivity of antinuclear antibody (ANA), anti-thyroid peroxidase (Anti-TPO) and anti-thyroglobulin (Anti-TG) antibodies. Based on these results, the patient with MS who has chronic autoimmune thyroiditis and primary ovarian failure was diagnosed with APS III. The coexistence of APS-III and MS is a rare clinical entity. Moreover, hypothyroidism has been detected during teriflunomide therapy in the patient. Hypothyroidism was most likely a component of APS-III in our case, but it may also have been triggered by teriflunomide. | en_US |
dc.identifier.citation | Gorgel, A., Tecellioglu, M., & Cankaya, C. (2021). Autoimmune polyglandular syndrome type III which accompanies to multiple sclerosis: A case report . Annals of Medical Research | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/54742 | |
dc.language.iso | en | en_US |
dc.relation.ispartof | Annals of Medical Research | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | Autoimmune polyglandular syndrome type III which accompanies to multiple sclerosis: A case report | en_US |
dc.type | Article | en_US |