Autoimmune Polyglandular Syndrome Type 2 Presentation With Alopecia Universalis, Hashimoto's Disease, and Addison's Disease

    Karla Denisse Sales-Morales, Nazhira Torres-Neme, Vladimir Barrera-Villanueva, Alejandro Martínez-Carreón
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    Studysummary This case study reported on a 30-year-old male with autoimmune polyglandular syndrome type 2, highlighting rare co-occurrence with alopecia universalis and emphasizing the importance of recognizing non-endocrine symptoms for early diagnosis and management of autoimmune endocrinopathies. Our plain-language summary of this paper — not a Tressless recommendation.
    This case report details a 30-year-old male with autoimmune polyglandular syndrome type 2 (APS2), presenting with alopecia universalis, Hashimoto’s disease, and Addison’s disease. APS2 is rare and involves primary adrenal insufficiency with autoimmune thyroid disease and/or type 1 diabetes. The case highlights the complexity of autoimmune diseases and the necessity of a multidisciplinary approach for effective diagnosis and management. It stresses the importance of timely recognition and treatment to prevent severe complications and improve quality of life, while also recommending ongoing monitoring for future comorbidities. The report notes the rarity of APS2's association with alopecia universalis, with only two other cases documented.
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