Why the study?
Adrenocortical oncocytic neoplasms are very rare among adrenal cortical tumors.
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Laparoscopic resection of a rare adrenocortical oncocytic neoplasm resulted in no recurrence at 11 months.
Adrenocortical oncocytic neoplasms (ACONs) are very rare in adrenal cortical tumors. One case was reported in this paper. During the physical examination, a soft tissue density shadow was about 6 cm × 5.7 cm in the right adrenal gland. A preoperative diagnosis was adrenal pheochromocytoma with concurrent laparoscopic resection of the right adrenal tumor. Postoperative pathological results rewarded the adrenal cortical oncocytic neoplasms ACONs. After 11-months of postoperative follow-up, the patient had no signs of tumor recurrence and related complications.
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Dong et al. (2025) studied this question.
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