A Case Report of Duodenal Psammomatous Somatostatinoma

Somatostatinoma is a neuroendocrine tumor; its incidence in the duodenum around the ampulla of Vater is rare, and it is often not associated with secretory manifestation. The authors report a case of a female with an ampullary (Vater) tumor displaying neuroendocrine nuclear features, psammoma bodies...

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Main Authors: Ayman Fisal Ahmed Foad, Hyder Osman Mirghani
Format: Article
Language:English
Published: Knowledge E 2018-09-01
Series:Sudan Journal of Medical Sciences
Online Access:https://doi.org/10.18502/sjms.v13i3.2956
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author Ayman Fisal Ahmed Foad
Hyder Osman Mirghani
author_facet Ayman Fisal Ahmed Foad
Hyder Osman Mirghani
author_sort Ayman Fisal Ahmed Foad
collection DOAJ
description Somatostatinoma is a neuroendocrine tumor; its incidence in the duodenum around the ampulla of Vater is rare, and it is often not associated with secretory manifestation. The authors report a case of a female with an ampullary (Vater) tumor displaying neuroendocrine nuclear features, psammoma bodies, and the positivity for immunohistochemical panel of neuroendocrine tumors. The patient was presented with some features compatible with somatostatin secretion-associated syndrome; albeit with normal serum levels of the hormone. Initial attempt of complete resection failed, and the involved margins were revised with a subsequent surgery, and the patient showed an uneventful course on follow-up for two years.
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spelling doaj.art-8bb7f64d02294b3786ba668919fb4b6a2022-12-21T22:11:30ZengKnowledge ESudan Journal of Medical Sciences1858-50512018-09-01131910.18502/sjms.v13i3.2956sjms.v13i3.2956A Case Report of Duodenal Psammomatous SomatostatinomaAyman Fisal Ahmed Foad0Hyder Osman Mirghani1 Department of Internal Medicine and Endocrine, Faculty of Medicine, University of Tabuk, Saudi Arabia Department of Internal Medicine and Endocrine, Faculty of Medicine, University of Tabuk, Saudi ArabiaSomatostatinoma is a neuroendocrine tumor; its incidence in the duodenum around the ampulla of Vater is rare, and it is often not associated with secretory manifestation. The authors report a case of a female with an ampullary (Vater) tumor displaying neuroendocrine nuclear features, psammoma bodies, and the positivity for immunohistochemical panel of neuroendocrine tumors. The patient was presented with some features compatible with somatostatin secretion-associated syndrome; albeit with normal serum levels of the hormone. Initial attempt of complete resection failed, and the involved margins were revised with a subsequent surgery, and the patient showed an uneventful course on follow-up for two years.https://doi.org/10.18502/sjms.v13i3.2956
spellingShingle Ayman Fisal Ahmed Foad
Hyder Osman Mirghani
A Case Report of Duodenal Psammomatous Somatostatinoma
Sudan Journal of Medical Sciences
title A Case Report of Duodenal Psammomatous Somatostatinoma
title_full A Case Report of Duodenal Psammomatous Somatostatinoma
title_fullStr A Case Report of Duodenal Psammomatous Somatostatinoma
title_full_unstemmed A Case Report of Duodenal Psammomatous Somatostatinoma
title_short A Case Report of Duodenal Psammomatous Somatostatinoma
title_sort case report of duodenal psammomatous somatostatinoma
url https://doi.org/10.18502/sjms.v13i3.2956
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