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Abstract
ABSTRACT
Ganglioneuroma (GN) is a rare benign tumor arising mainly from neural crest cells and consisting of Schwann and ganglion cells. GN rarely occurs from the adrenal medulla and is observed most commonly in children and young adults. It is not associated with hormonal activity and is clinically asymptomatic. We present a 35-year-old woman whose abdominal ultrasonography for abdominal pain revealed in the rightadrenal gland, a biochemically normal mass that was minimally hypointense on T1-weighted and hyperintense on T2-weighted magnetic resonance images (MRI) and which was pathologically diagnosed as GN after adrenalectomy.
Article Info
Published In
Journal
Endocrinology Research and Practice
Volume / Issue
Volume 15 · Issue 3
Pages
74-76
History
Published Online
September 1, 2011
Copyright
Copyright (c) 2011 Endocrinology Research and Practice
Affiliations
Fatih Kılıçlı
Cumhuriyet University, Faculty of Medicine, Department of Endocrinology and Metabolism, Sivas, Turkey
Fettah Acıbucu
Cumhuriyet University, Faculty of Medicine, Department of Endocrinology and Metabolism, Sivas, Turkey
Hatice Sebila Dökmetaş
Cumhuriyet University, Faculty of Medicine, Department of Endocrinology and Metabolism, Sivas, Turkey
Şahande Elagöz
Cumhuriyet University Faculty of Medicine, Department of Pathology, Sivas, Turkey
Gökhan Gökçe
Cumhuriyet University Faculty of Medicine, Department of Urology, Sivas, Turkey
İbrahim Öztoprak
Cumhuriyet University Faculty of Medicine, Department of Radiology, Sivas, Turkey
Cite this Article
Kılıçlı, F., Acıbucu, F., Dökmetaş, H. S., Elagöz, Şahande, Gökçe, G., & Öztoprak, İbrahim. (2011). Adrenal Ganglioneuroma: Case Report. Endocrinology Research and Practice, 15(3), 74–76. Retrieved from https://endocrinolrespract.org/index.php/pub/article/view/599
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