References
- Cairns P. Renal cell carcinoma. Cancer Biomark. 2010;9(1–6):461–473.
- Lenders N, Greenfield J. Urinary steroid profiling in diagnostic evaluation of an unusual adrenal mass. Endocrinol Diabetes Metabol Case Rep. 2019;2019:19–0090.
- Kakimoto S, Yushita Y, Sanefuji T, et al. Non-hormonal adrenocortical adenoma with oncocytoma-like appearances. Hinyokika Kiyo. 1986;32(5):757–763.
- Chang A, Harawi S. Oncocytes, oncocytosis, and oncocytic tumors. Pathology Annual. 1992;27:263–304.
- Smirnova E, Mikhaĭlov I. Electron microscopic characteristics of oncocytoma of the lung, small intestine and adrenal gland. Arkhivv Pathologii. 1986;48:79–81.
- Hong Y, Hao Y, Hu J, et al. Adrenocortical oncocytoma: 11 case reports and review of the literature. Medicine. 2017;96(48):e8750.
- Nosé V. Diagnostic pathology. 2nd ed. Philadelphia (PA): Elsevier; 2018. p. 459.
- Mearini L, Del Sordo R, Costantini E, et al. Adrenal oncocytic neoplasm: a systematic review. Urol Int. 2013;91(2):125–133.
- Wong D, Spagnolo D, Bisceglia M, et al. Oncocytic adrenocortical neoplasms—a clinicopathologic study of 13 new cases emphasizing the importance of their recognition. Hum Pathol. 2011;42(4):489–499.
- Fuhrman S, Lasky L, Limas C. Prognostic significance of morphologic parameters in renal cell carcinoma. Am J Surg Pathol. 1982;6(7):655–664.
- Weiss L. Comparative histologic study of 43 metastasizing and nonmetastasizing adrenocortical tumors. Am J Surg Pathol. 1984;8(3):163–170.
- Jain M, Kapoor S, Mishra A, et al. Weiss criteria in large adrenocortical tumors: a validation study. Indian J Pathol Microbiol. 2010;53(2):222–226.
- Bisceglia M, Ludovico O, Di Mattia A, et al. Adrenocortical oncocytic tumors: report of 10 cases and review of the literature. Int J Surg Pathol. 2004;12(3):231–243.
- Alamoudi O, Alsulaiman W, Aldhaam N, et al. Incidental finding of adrenal oncocytoma after right robotic adrenalectomy: case report and literature review. Urol Case Rep. 2017;12:14–16.
- Bhattarai R, Savino R, Dhakal B, et al. Adrenocortical oncocytoma with borderline malignant potential causing subclinical cushing syndrome. AACE Clinical Case Reports. 2017;3(1):e46–e50.