Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma

Background. Adrenal collision tumors (ACTs), in which distinct tumors coexist without intermingling in the same adrenal gland, are rare and their actual prevalence is unknown. ACTs commonly consist of adrenal cortical adenoma, pheochromocytoma, or metastatic malignant tumor. Case Report. A 32-year-o...

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Main Authors: Hye Seung Lee, Yoo Jin Choi, Chungyeul Kim, Baek-Hui Kim
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Case Reports in Surgery
Online Access:http://dx.doi.org/10.1155/2016/5790645
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spelling doaj-44c56ed2e09048439030c8a65beb53732020-11-25T01:57:55ZengHindawi LimitedCase Reports in Surgery2090-69002090-69192016-01-01201610.1155/2016/57906455790645Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and GanglioneuromaHye Seung Lee0Yoo Jin Choi1Chungyeul Kim2Baek-Hui Kim3Department of Pathology, Korea University School of Medicine, Seoul, Republic of KoreaDepartment of Pathology, Korea University School of Medicine, Seoul, Republic of KoreaDepartment of Pathology, Korea University School of Medicine, Seoul, Republic of KoreaDepartment of Pathology, Korea University School of Medicine, Seoul, Republic of KoreaBackground. Adrenal collision tumors (ACTs), in which distinct tumors coexist without intermingling in the same adrenal gland, are rare and their actual prevalence is unknown. ACTs commonly consist of adrenal cortical adenoma, pheochromocytoma, or metastatic malignant tumor. Case Report. A 32-year-old woman who had been experiencing gastric discomfort for one month was referred to our hospital with abnormal imaging findings. The physical examination and the laboratory data including endocrine studies were unremarkable. Abdomen computed tomography (CT) and magnetic resonance imaging (MRI) showed two adjacent masses in the left suprarenal fossa, and a laparoscopic left adrenalectomy was done. Histological and immunohistochemical (IHC) examinations revealed two distinct tumors: a pigmented adrenal cortical oncocytoma (ACO) and a ganglioneuroma, respectively. Conclusion. Both tumors are rare in the adrenal gland and exist as ACTs only exceptionally rarely. This is the first reported case of coexisting oncocytoma and ganglioneuroma in the same adrenal gland to our knowledge.http://dx.doi.org/10.1155/2016/5790645
collection DOAJ
language English
format Article
sources DOAJ
author Hye Seung Lee
Yoo Jin Choi
Chungyeul Kim
Baek-Hui Kim
spellingShingle Hye Seung Lee
Yoo Jin Choi
Chungyeul Kim
Baek-Hui Kim
Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma
Case Reports in Surgery
author_facet Hye Seung Lee
Yoo Jin Choi
Chungyeul Kim
Baek-Hui Kim
author_sort Hye Seung Lee
title Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma
title_short Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma
title_full Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma
title_fullStr Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma
title_full_unstemmed Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma
title_sort adrenal collision tumor: coexistence of pigmented adrenal cortical oncocytoma and ganglioneuroma
publisher Hindawi Limited
series Case Reports in Surgery
issn 2090-6900
2090-6919
publishDate 2016-01-01
description Background. Adrenal collision tumors (ACTs), in which distinct tumors coexist without intermingling in the same adrenal gland, are rare and their actual prevalence is unknown. ACTs commonly consist of adrenal cortical adenoma, pheochromocytoma, or metastatic malignant tumor. Case Report. A 32-year-old woman who had been experiencing gastric discomfort for one month was referred to our hospital with abnormal imaging findings. The physical examination and the laboratory data including endocrine studies were unremarkable. Abdomen computed tomography (CT) and magnetic resonance imaging (MRI) showed two adjacent masses in the left suprarenal fossa, and a laparoscopic left adrenalectomy was done. Histological and immunohistochemical (IHC) examinations revealed two distinct tumors: a pigmented adrenal cortical oncocytoma (ACO) and a ganglioneuroma, respectively. Conclusion. Both tumors are rare in the adrenal gland and exist as ACTs only exceptionally rarely. This is the first reported case of coexisting oncocytoma and ganglioneuroma in the same adrenal gland to our knowledge.
url http://dx.doi.org/10.1155/2016/5790645
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AT yoojinchoi adrenalcollisiontumorcoexistenceofpigmentedadrenalcorticaloncocytomaandganglioneuroma
AT chungyeulkim adrenalcollisiontumorcoexistenceofpigmentedadrenalcorticaloncocytomaandganglioneuroma
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