Adrenal oncocytoma: an unusual etiology of Cushing’s syndrome in an adolescent female
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Saba Samad Memon
, Manjunath Havalappa Dodamani, Sanjay Chaudhari
, Zalak Parmar
, Kaushal Patel
, Suresh Bhoi and Ravikumar Shah
Abstract
Objectives
This report presents a rare pediatric functional AO causing CS and androgen excess. It aims to discuss the diagnostic challenges of cortisol and DHEAS co-secretion, which may mimic adenomas or carcinomas. It also emphasizes the role of clinical, biochemical, and imaging assessments, as well as histological classification using LWB criteria, and the need for long-term follow-up.
Case presentation
A 17-year-old female presented with weight gain, moon facies, cushingoid striae, oligomenorrhea, and acne over six months. Examination showed hypertension, grade I obesity, cushingoid stigmata without virilization. Endocrine evaluation was confirmed ACTH independent CS due to right AO.
Conclusions
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.
Acknowledgments
Ms. Palak Raj-helped in retrieving the case details and prepare the manuscript.
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Research ethics: Not applicable.
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Informed consent: Informed consent was obtained from their legal guardians.
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Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: Not applicable.
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Conflict of interest: The authors state no conflict of interest.
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Research funding: None declared.
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Data availability: Not applicable.
References
1. Ferrigno, R, Hasenmajer, V, Caiulo, S, Minnetti, M, Mazzotta, P, Storr, HL, et al.. Paediatric Cushing’s disease: epidemiology, pathogenesis, clinical management and outcome. Rev Endocr Metab Disord 2021;22:817–35. https://doi.org/10.1007/s11154-021-09626-4.Search in Google Scholar PubMed PubMed Central
2. Arnaldi, G, Martino, M. Androgens in cushing’s syndrome. Front Horm Res 2019;53:77–91. https://doi.org/10.1159/000494904.Search in Google Scholar PubMed
3. Kovacic, J, Louie-Johnsun, M. A rare case of co-secreting adrenocortical oncocytoma. Urol Case Rep 2023;46:102285. https://doi.org/10.1016/j.eucr.2022.102285.Search in Google Scholar PubMed PubMed Central
4. Coppola Bottazzi, E, Gambardella, C, Mongardini, FM, Vanella, S, Noviello, A, Palma, T, et al.. Prognosis of adrenal oncocytic neoplasms (AONs): literature review of 287 cases and presentation of the oldest patient. J Clin Med 2023;12:6925. https://doi.org/10.3390/jcm12216925.Search in Google Scholar PubMed PubMed Central
5. Dong, D, Liu, X, Ji, Z, Li, H. Diagnosis and treatment of adrenocortical oncocytoma: case report of five cases and review of the literature. Front Oncol 2019;9:338. https://doi.org/10.3389/fonc.2019.00338.Search in Google Scholar PubMed PubMed Central
6. Subbiah, S, Nahar, U, Samujh, R, Bhansali, A. Heterosexual precocity: rare manifestation of virilizing adrenocortical oncocytoma. Ann Saudi Med 2013;33:294–7. https://doi.org/10.5144/0256-4947.2013.294.Search in Google Scholar PubMed PubMed Central
7. Al Badi, MK, Al-Alwan, I, Al-Dubayee, M, Al-Anzi, A, Al Turki, MS, Aloudah, N, et al.. Testosterone- and cortisol-secreting oncocytic adrenocortical adenoma in the pediatric age-group. Pediatr Dev Pathol 2018;21:568–73. https://doi.org/10.1177/1093526617753045.Search in Google Scholar PubMed
8. Narayanan, N, Kamalanathan, S, Sahoo, J, Naik, D, Kumaravel, S, Ganesh, RN. Pediatric adrenocortical oncocytoma presenting as cushing’s syndrome and peripheral precocious puberty: a case report and review of literature. J Asean Fed Endocr Soc 2021;36:205–8. https://doi.org/10.15605/jafes.036.02.17.Search in Google Scholar PubMed PubMed Central
9. Gadelha, M, Gatto, F, Wildemberg, LE, Fleseriu, M. Cushing’s syndrome. Lancet 2023;402:2237–52. https://doi.org/10.1016/S0140-6736(23)01961-X.Search in Google Scholar PubMed
10. Goroshi, M, Jadhav, SS, Sarathi, V, Lila, AR, Patil, VA, Shah, R, et al.. Radiological differentiation of phaeochromocytoma from other malignant adrenal masses: importance of wash-in characteristics on multiphase CECT. Endocr Connect 2019;8:898–905. https://doi.org/10.1530/EC-19-0198.Search in Google Scholar PubMed PubMed Central
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Articles in the same Issue
- Frontmatter
- Review
- Prevalence of congenital hypothyroidism in infants of mothers with hypothyroidism: a meta-analysis
- Original Articles
- Pubertal characteristics, final height, and associated factors in patients with nonclassical congenital adrenal hyperplasia: a single center experience
- Serum α-Klotho and its association with testosterone in boys with central precocious puberty
- Bioelectrical impedance analysis and hormonal assessment in adolescents with pubertal gynecomastia
- The relationship between FSTL-1 (follistatin-related protein 1), FAM19A5 (family with sequence similarity 19, member A5) and CTRP-6 (C1q/TNF-related protein 6) levels and metabolic parameters in overweight children
- Role of hyperandrogenism on disordered eating behaviors in adolescents with PCOS and interplay with insulin resistance
- The impact of hepatic steatosis on epicardial adipose tissue in obese individuals
- Exploratory real-world experience with GLP-1 receptor agonists vs. metformin in youth with new-onset type 2 diabetes: a single-center retrospective study
- Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity
- Short Communication
- Implementation and feasibility of a nutrition assessment for recently diagnosed youth with type 2 diabetes
- Case Reports
- Noonan syndrome and autoimmune hepatitis: patient report and literature review
- Adrenal oncocytoma: an unusual etiology of Cushing’s syndrome in an adolescent female
- Novel MCT8 mutation: diagnostic value of T3/T4 ratio
- Clinical insights of the TBX19 C.856 C>T variant: a case report and literature review on neonatal isolated ACTH deficiency
- Wolcott–Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene