Adrenal oncocytoma: an unusual etiology of Cushing’s syndrome in an adolescent female
This case illustrates functional AO as a rare cause of adolescent CS with androgen excess. Co-secretion patterns complicate diagnosis, imaging may not be definitive, and long-term follow-up is vital due to uncertain prognosis.
Authors
- Ravikumar Shah (ORCID: https://orcid.org/0000-0001-6275-5650)
- Sanjeev Kumar Bhoi (ORCID: https://orcid.org/0000-0002-5192-7637)
- Manjunath Havalappa Dodamani (ORCID: https://orcid.org/0000-0002-6658-0269)
- Saba Samad Memon (ORCID: https://orcid.org/0000-0001-5199-6299)
- Sanjay Chaudhari (ORCID: https://orcid.org/0000-0001-6627-4942)
- Kaushal Patel (ORCID: https://orcid.org/0009-0007-1098-3150)
- Zalak Parmar (ORCID: https://orcid.org/0000-0002-8363-7773)
Institutions
- King Edward Memorial Hospital and Seth G.S. Medical College (IN)
- Gujarat Kidney Foundation (IN)
- Pramukhswami Medical College (IN)
- Diabetes Care & Hormone Clinic (IN)
- Nethradhama Superspeciality Eye Hospital (IN)
Publication Details
- Journal
- Journal of Pediatric Endocrinology and Metabolism
- Published
- 2025-09-30
- DOI
- https://doi.org/10.1515/jpem-2025-0369
- Primary Topic
- Pituitary Gland Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00