Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour

Oncocytic neoplasms are well recognized in organs such as the kidney, thyroid and salivary glands. They are seen rarely in other sites such as the adrenal cortex. To date, around 20 cases of oncocytic adrenocortical neoplasm have been reported; most of them were benign and nonfunctioning. We report...

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Main Authors: Abhishek Singhai, Subodh Banzal
Format: Article
Language:English
Published: SpringerOpen 2014-01-01
Series:The Egyptian Journal of Internal Medicine
Subjects:
Online Access:http://www.esim.eg.net/article.asp?issn=1110-7782;year=2014;volume=26;issue=4;spage=184;epage=185;aulast=Singhai
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author Abhishek Singhai
Subodh Banzal
author_facet Abhishek Singhai
Subodh Banzal
author_sort Abhishek Singhai
collection DOAJ
description Oncocytic neoplasms are well recognized in organs such as the kidney, thyroid and salivary glands. They are seen rarely in other sites such as the adrenal cortex. To date, around 20 cases of oncocytic adrenocortical neoplasm have been reported; most of them were benign and nonfunctioning. We report the case of hypersecreting adrenocortical oncocytoma in a 52-year-old woman. The patient was tested because of cushingoid features. The patient underwent a laparotomy for right adrenal gland mass. The pathology report confirmed adrenocortical oncocytoma.
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spelling doaj.art-db8497aa708f4020b427b795f0e954fc2022-12-22T03:01:17ZengSpringerOpenThe Egyptian Journal of Internal Medicine1110-77822090-90982014-01-0126418418510.4103/1110-7782.148180Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumourAbhishek SinghaiSubodh BanzalOncocytic neoplasms are well recognized in organs such as the kidney, thyroid and salivary glands. They are seen rarely in other sites such as the adrenal cortex. To date, around 20 cases of oncocytic adrenocortical neoplasm have been reported; most of them were benign and nonfunctioning. We report the case of hypersecreting adrenocortical oncocytoma in a 52-year-old woman. The patient was tested because of cushingoid features. The patient underwent a laparotomy for right adrenal gland mass. The pathology report confirmed adrenocortical oncocytoma.http://www.esim.eg.net/article.asp?issn=1110-7782;year=2014;volume=26;issue=4;spage=184;epage=185;aulast=SinghaiAdrenal gland, cushing syndrome, oncocytoma
spellingShingle Abhishek Singhai
Subodh Banzal
Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
The Egyptian Journal of Internal Medicine
Adrenal gland, cushing syndrome, oncocytoma
title Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
title_full Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
title_fullStr Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
title_full_unstemmed Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
title_short Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
title_sort oncocytic adrenal tumour presenting as cushing syndrome rare presentation of a rare tumour
topic Adrenal gland, cushing syndrome, oncocytoma
url http://www.esim.eg.net/article.asp?issn=1110-7782;year=2014;volume=26;issue=4;spage=184;epage=185;aulast=Singhai
work_keys_str_mv AT abhisheksinghai oncocyticadrenaltumourpresentingascushingsyndromerarepresentationofararetumour
AT subodhbanzal oncocyticadrenaltumourpresentingascushingsyndromerarepresentationofararetumour