Autoimmune Polyglandular Syndrome Type 2 With Hurthle Cell Adenoma: A Rare Association

Shalini S Pandya1, Kush Shah2, Hitesh Chavda3

  • 1Department of Internal Medicine, Sterling Hospitals, Ahmedabad, IND.

Cureus
|October 24, 2025
PubMed
Summary

Autoimmune Polyglandular Syndrome type 2 (APS 2) is rare, often diagnosed late. This case highlights a unique co-occurrence with Hurthle cell adenoma, emphasizing diagnostic vigilance and management of this rare endocrinopathy.

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