A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma

Adrenocortical oncocytomas are extremely rare, usually incidentally detected tumors that are thought to have low malignant potential. The number of reported cases in the literature is below 200. These tumors are frequently non-functional and do not secrete hormones, but cases of oncocytoma causing h...

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Main Authors: Serdar Aslan, Mehmet Selim Nural
Format: Article
Language:English
Published: Galenos Yayinevi 2019-12-01
Series:Journal of Urological Surgery
Subjects:
Online Access: http://jurolsurgery.org/archives/archive-detail/article-preview/a-rare-cause-of-adrenal-mass-adrenocortical-oncocy/31932
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author Serdar Aslan
Mehmet Selim Nural
author_facet Serdar Aslan
Mehmet Selim Nural
author_sort Serdar Aslan
collection DOAJ
description Adrenocortical oncocytomas are extremely rare, usually incidentally detected tumors that are thought to have low malignant potential. The number of reported cases in the literature is below 200. These tumors are frequently non-functional and do not secrete hormones, but cases of oncocytoma causing hypertension, Cushing syndrome, and virilization have also been reported. Imaging methods are insufficient for diagnosis, and a definitive diagnosis can only be made after a histopathological examination of the adrenalectomy specimen. Here, we present the imaging and histopathological features of an adrenal mass in a 46-year-old woman who presented with left renal colic.
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spelling doaj.art-af59225fcdde4038aadedd62151dd78d2023-02-15T16:21:48ZengGalenos YayineviJournal of Urological Surgery2148-95802148-95802019-12-016433533810.4274/jus.galenos.2019.282513049054A Rare Cause of Adrenal Mass: Adrenocortical OncocytomaSerdar Aslan0Mehmet Selim Nural1 Giresun University Faculty of Medicine, Department of Radiology, Giresun, Turkiye Ondokuz Mayıs University Faculty of Medicine, Department of Radiology, Samsun, Turkiye Adrenocortical oncocytomas are extremely rare, usually incidentally detected tumors that are thought to have low malignant potential. The number of reported cases in the literature is below 200. These tumors are frequently non-functional and do not secrete hormones, but cases of oncocytoma causing hypertension, Cushing syndrome, and virilization have also been reported. Imaging methods are insufficient for diagnosis, and a definitive diagnosis can only be made after a histopathological examination of the adrenalectomy specimen. Here, we present the imaging and histopathological features of an adrenal mass in a 46-year-old woman who presented with left renal colic. http://jurolsurgery.org/archives/archive-detail/article-preview/a-rare-cause-of-adrenal-mass-adrenocortical-oncocy/31932 adrenal glandadrenal oncocystomacomputed tomography
spellingShingle Serdar Aslan
Mehmet Selim Nural
A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma
Journal of Urological Surgery
adrenal gland
adrenal oncocystoma
computed tomography
title A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma
title_full A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma
title_fullStr A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma
title_full_unstemmed A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma
title_short A Rare Cause of Adrenal Mass: Adrenocortical Oncocytoma
title_sort rare cause of adrenal mass adrenocortical oncocytoma
topic adrenal gland
adrenal oncocystoma
computed tomography
url http://jurolsurgery.org/archives/archive-detail/article-preview/a-rare-cause-of-adrenal-mass-adrenocortical-oncocy/31932
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