Journal List > Korean J Urol > v.48(1) > 1004796

Chang, Sohn, Park, Kim, and Kwon: Adrenocortical Oncocytoma

Abstract

An adrenocortical oncocytoma is very rare and unusual disease. Only 22 and 2 cases have been reported in the foreign and Korean literatures, respectively. Herein, the case of a left adrenocortical oncocytoma, observed by ultrasonography during a periodic medical examination of a 32 year old male patient is reported.

Figures and Tables

Fig. 1
T2-weighted magnetic resonance imaging of the abdomen. The left adrenal tumor was separated from the left kidney and enclosed by a capsule.
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Fig. 2
Left adrenal tumor: solid mass separated from the residual adrenal gland.
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Fig. 3
Typical structure of an oncocytoma, with abundant eosinophilic cytoplasm (H&E, ×40), small picture (H&E, ×200) (A). Very low Ki-67 labelling index (Immunostaining, ×200) (B).
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Fig. 4
Electron microscopy: closely packed mitochondria, with an electron dense inclusion (×5,000).
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References

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