Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review

Autoimmune polyglandular syndromes (APS) are rare disorders characterized by auto‐destruction of endocrine and non‐endocrine organs by organ‐specific antibody‐directed T‐lymphocytic infiltration. This case highlights a 29‐year‐old Caucasian man with vitiligo found to have significant neurological ab...

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Detalles Bibliográficos
Autores principales: Apolinario, Michael, Brussels, Aaron, Cook, Curtiss B., Yang, Shaun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815091/
https://www.ncbi.nlm.nih.gov/pubmed/35140971
http://dx.doi.org/10.1002/ccr3.5391
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author Apolinario, Michael
Brussels, Aaron
Cook, Curtiss B.
Yang, Shaun
author_facet Apolinario, Michael
Brussels, Aaron
Cook, Curtiss B.
Yang, Shaun
author_sort Apolinario, Michael
collection PubMed
description Autoimmune polyglandular syndromes (APS) are rare disorders characterized by auto‐destruction of endocrine and non‐endocrine organs by organ‐specific antibody‐directed T‐lymphocytic infiltration. This case highlights a 29‐year‐old Caucasian man with vitiligo found to have significant neurological abnormalities in the setting of newly diagnosed pernicious anemia and thyroid autoimmune disease.
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spelling pubmed-88150912022-02-08 Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review Apolinario, Michael Brussels, Aaron Cook, Curtiss B. Yang, Shaun Clin Case Rep Case Reports Autoimmune polyglandular syndromes (APS) are rare disorders characterized by auto‐destruction of endocrine and non‐endocrine organs by organ‐specific antibody‐directed T‐lymphocytic infiltration. This case highlights a 29‐year‐old Caucasian man with vitiligo found to have significant neurological abnormalities in the setting of newly diagnosed pernicious anemia and thyroid autoimmune disease. John Wiley and Sons Inc. 2022-02-04 /pmc/articles/PMC8815091/ /pubmed/35140971 http://dx.doi.org/10.1002/ccr3.5391 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Apolinario, Michael
Brussels, Aaron
Cook, Curtiss B.
Yang, Shaun
Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review
title Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review
title_full Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review
title_fullStr Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review
title_full_unstemmed Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review
title_short Autoimmune polyglandular syndrome type 3: A case report of an unusual presentation and literature review
title_sort autoimmune polyglandular syndrome type 3: a case report of an unusual presentation and literature review
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815091/
https://www.ncbi.nlm.nih.gov/pubmed/35140971
http://dx.doi.org/10.1002/ccr3.5391
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AT cookcurtissb autoimmunepolyglandularsyndrometype3acasereportofanunusualpresentationandliteraturereview
AT yangshaun autoimmunepolyglandularsyndrometype3acasereportofanunusualpresentationandliteraturereview

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