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Case Reports
. 2015 Jan-Feb;77(1):55-59.
doi: 10.17116/patol201577155-.

[Adrenocortical oncocytoma]

[Article in Russian]
L S Selivanova  1 , F M Abdulkhabirova  2 , I A Voronkova  2 , N S Kuznetsov  2 , E A Troshina  2 , A O Raikhman  2 , T M Birg  3 , A S Tertychnyi  3
Affiliations
Case Reports

[Adrenocortical oncocytoma]

[Article in Russian]
L S Selivanova et al. Arkh Patol. 2015 Jan-Feb.

Abstract
in English, Russian

The paper characterizes adrenocortical oncocytoma, a rare adrenal tumor, accompanied by Cushing's syndrome and estrogen and androgen production and provides histological and immunohistochemical features. The authors describe their observation of a 33-year-old female woman. It is shown that estimation of the malignant potential of adrenocortical oncocytomas requires a special approach and must be done using the Lin-Weiss-Bisceglia criteria.

Представлена характеристика редкой адренокортикальной опухоли надпочечника - онкоцитомы, сопровождающейся синдромом Кушинга, продукцией эстрогенов и андрогенов, включая гистологические, иммуногистохимические характеристики. Приведено собственное наблюдение больной 33 лет. Показано, что оценка злокачественного потенциала адренокортикальных онкоцитарных опухолей надпочечника требует особого подхода и должна проводиться по критериям, предложенным Lin-Weiss-Bisceglia.

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