Korean J Urol.  2009 Apr;50(4):401-403.

A Functioning Adrenocortical Oncocytoma

Affiliations
  • 1Department of Urology, School of Medicine, Kyungpook National University, Daegu, Korea. tgkwon@knu.ac.kr
  • 2Department of Pathology, School of Medicine, Kyungpook National University, Daegu, Korea.

Abstract

Adrenocortical oncocytomas are exceptionally rare and most are benign and nonfunctioning. Only 3 cases of adrenal oncocytomas have been reported in the Korean literature and all of them were nonfunctioning. Herein, we report a case of a functioning adrenocortical oncocytoma in a 49-year-old man who presented with Cushing syndrome.

Keyword

Oxyphilic adenoma; Cushing syndrome

MeSH Terms

Adenoma, Oxyphilic
Cushing Syndrome
Humans
Middle Aged

Figure

  • Fig. 1 Enhanced abdominopelvic computed tomography. A 7.7 cm mass enclosed by a capsule was found on the left adrenal gland (A). Some necrotic tissue was found in the mass (B).

  • Fig. 2 Whole-body positron emission tomography/computed tomography (PET/CT) scan. A 7.7 cm hypermetabolic mass lesion with fluorodeoxyglucose (FDG) uptake was found in the left adrenal gland.

  • Fig. 3 The tumor was grossly well circumscribed with a dark brown color.

  • Fig. 4 Typical structure of an oncocytoma with abundant eosinophilic and granular cytoplasm. Nuclear atypia with enlarged nuclei was found (H&E, ×200).

  • Fig. 5 Electron microscopy. Electron dense inclusion and closely packed mitochondria were found. Some destructed mitochondria with Golgi complex were found (×4,000).


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