Case of autoimmune polyglandular syndrome type 2: how we uncovered the diagnosis
- PMID: 30814097
- PMCID: PMC6398778
- DOI: 10.1136/bcr-2018-227187
Case of autoimmune polyglandular syndrome type 2: how we uncovered the diagnosis
Abstract
A 24-year-old man with no significant medical history presented to the medical clinic with vomiting and giddiness for 2 days, loss of appetite for 1 month and progressive fatigability for the preceding 4 months. On examination, he was found to be hypotensive and was admitted to the hospital for work-up. Considering his abnormal labs and physical findings, he was worked up and was diagnosed with primary adrenal insufficiency. On further work-up for the aetiology of his Addison's disease, he was found to have concurrent autoimmune thyroiditis and vitiligo. A final diagnosis of autoimmune polyglandular syndrome type 2 was made. The patient was started on hormone replacement therapy and reported improvement of symptoms on 3-month follow-up visit.
Keywords: adrenal disorders; endocrinology; immunology; thyroid disease.
© BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.
Conflict of interest statement
Competing interests: None declared.
Figures
References
-
- Schmidt MB. Eine biglandulare Erkrankung (Nebennieren und Schilddruse bei Morbus Addisonni). Dtsch Pathol Ges 1926;21:212–21.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources