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Adreno-cortical oncocytoma: a case report.
Ibtissem Bouasker1, Ayoub Zoghlami, Faten Farah Klibi
1Service de Chirurgie Générale B, Hôpital Charles Nicolle, Tunis, Tunisie.
La Tunisie Medicale
|June 3, 2010
Summary
Adrenal oncocytoma, a rare adrenal tumor, was diagnosed in a 72-year-old man. Surgical removal resulted in a good prognosis with no recurrence after 8 months.
Area of Science:
- Endocrinology
- Oncology
- Surgical Pathology
Background:
- Adrenal oncocytoma is an exceptionally rare adrenal gland neoplasm.
- Most adrenal oncocytomas are non-functioning and benign, with fewer than 50 cases reported historically.
Observation:
- A 72-year-old male presented with renal fossa pain.
- Imaging revealed a large right adrenal mass extending into the right kidney.
- Surgical resection included right adrenalectomy and nephrectomy.
Findings:
- Pathological diagnosis confirmed adrenal oncocytoma with uncertain malignant potential.
- The patient experienced an uncomplicated recovery and was discharged on postoperative day five.
- Eight months of follow-up showed no evidence of tumor recurrence.
Implications:
- This case contributes to the limited literature on adrenal oncocytoma.
- Adrenocortical oncocytomas, despite potential malignancy concerns, appear to have a favorable prognosis following surgical management.
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