Pediatric Adrenocortical Oncocytoma Presenting As Cushing's Syndrome and Peripheral Precocious Puberty: A Case Report and Review of Literature
Overview
Authors
Affiliations
Oncocytic adrenocortical tumours (OATs) or oncocytomas are extremely rare and are usually benign and nonfunctional. We report the case of a 4-year-old male with a right-sided, functional oncocytic adrenocortical adenoma, who presented with precocious puberty and Cushing's syndrome. After work-up, the patient underwent laparoscopic adrenalectomy. The excised adrenal mass weighed 21 g and measured 3.5 cm in maximum dimension. Histological examination demonstrated no features suggestive of aggressive biological behaviour. The patient had no features of recurrent or metastatic disease and had prepubertal testosterone levels with suppressed hypothalamic-pituitary-adrenal axis twelve months after the surgery. A discussion of this case and a review of the literature on functional OATs in the pediatric population are presented.
Androgen producing oncocytic adrenocortical tumor in a 3.7-year-old female.
Mans K, Elmahmudi G, Bedrnicek J, Cabrera M Endocrinol Diabetes Metab Case Rep. 2025; 2025(1).
PMID: 39960756 PMC: 11850039. DOI: 10.1530/EDM-24-0143.
Case of clear-cell oncocytoma of parotid gland and literature review.
Zhu W, Zhang Y, Li F, Li G, Zhang P, Fang H Hua Xi Kou Qiang Yi Xue Za Zhi. 2024; 42(1):126-134.
PMID: 38475961 PMC: 10965352. DOI: 10.7518/hxkq.2024.2023185.
Cushing's syndrome caused by adrenocortical oncocytoma: A case report.
Gou C, Jian Q, Tian M, Li J, Zhang Y, Guo Z Oncol Lett. 2024; 27(4):177.
PMID: 38464335 PMC: 10921264. DOI: 10.3892/ol.2024.14310.
San Juan M, Lagamayo D, Carnate J, Joven M BMJ Case Rep. 2022; 15(4).
PMID: 35444021 PMC: 9021750. DOI: 10.1136/bcr-2021-248525.