Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma

Introduction. Brunner’s gland hamartomas are very uncommon. They are small, benign lesions, frequently located in the bulb of the duodenum. Usually found incidentally during routine esophago-gastro-duodenoscopies, these lesions are frequently asymptomatic, but some patients may present with symptoms...

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Main Authors: Gelu C. Rosianu, Anca Evsei, Mircea Gheorghe, Adelina Birceanu-Corobea, Narcis Copca
Format: Article
Language:English
Published: Balkan Medical Union 2017-12-01
Series:Archives of the Balkan Medical Union
Subjects:
Online Access:http://umbalk.org/wp-content/uploads/2017/12/14.ENDOSCOPIC-MANAGEMENT-OF-A-RARE-CASE.pdf
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spelling doaj-92011208f848418c9971e2180c4db1d22020-11-25T01:47:18ZengBalkan Medical UnionArchives of the Balkan Medical Union1584-92442558-815X2017-12-01524453457Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartomaGelu C. Rosianu0Anca Evsei1Mircea Gheorghe2Adelina Birceanu-Corobea3Narcis Copca4CESITO Center, „Sfanta Maria“ Clinical Hospital, Bucharest, Romania, Department of Gastroenterology, „Sfanta Maria“ Clinical Hospital, Bucharest, RomaniaCESITO Center, „Sfanta Maria“ Clinical Hospital, Bucharest, Romania,Department of Pathology, „Sfanta Maria“ Clinical Hospital, Bucharest, RomaniaDepartment of Surgery, „Sfanta Maria“ Clinical Hospital, Bucharest, RomaniaDepartment of Pathology, „Sfanta Maria“ Clinical Hospital, Bucharest, RomaniaDepartment of Surgery, „Sfanta Maria“ Clinical Hospital, Bucharest, RomaniaIntroduction. Brunner’s gland hamartomas are very uncommon. They are small, benign lesions, frequently located in the bulb of the duodenum. Usually found incidentally during routine esophago-gastro-duodenoscopies, these lesions are frequently asymptomatic, but some patients may present with symptoms of duodenal obstruction or hemorrhage secondary to ulceration. Surgical excision is required, especially if the lesion has large dimensions. The pathological examination is the most important in confirming the diagnosis.Case presentation. We report a case of a 64-year-old female patient, who presented to the emergency room for vomiting partially digested food, without blood. Upper digestive endoscopy revealed a polypoid mass, with a 1 cm stalk, located in the duodenal bulb. The polyp was successfully endoscopically resected and the pathological diagnosis was of Brunner’s gland hamartoma. Histologically, this polyp consisted of the components of Brunner’s gland cells, as well as glandular, adipose and muscle cells. Conclusions. Brunner’s gland hamartomas are rare duodenal tumors occurring in middle-aged patients that present either with gastrointestinal hemorrhage, obstructive symptoms or as an incidental finding. Surgical or endoscopic excision is uncomplicated, and the long-term outcome is favorable. The particularity of our case is given by the fact that this lesion was very large, it caused symptoms such as vomiting and was managed solely by endoscopic resection.http://umbalk.org/wp-content/uploads/2017/12/14.ENDOSCOPIC-MANAGEMENT-OF-A-RARE-CASE.pdfgiant hamartomaBrunner's glandendoscopic resection
collection DOAJ
language English
format Article
sources DOAJ
author Gelu C. Rosianu
Anca Evsei
Mircea Gheorghe
Adelina Birceanu-Corobea
Narcis Copca
spellingShingle Gelu C. Rosianu
Anca Evsei
Mircea Gheorghe
Adelina Birceanu-Corobea
Narcis Copca
Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma
Archives of the Balkan Medical Union
giant hamartoma
Brunner's gland
endoscopic resection
author_facet Gelu C. Rosianu
Anca Evsei
Mircea Gheorghe
Adelina Birceanu-Corobea
Narcis Copca
author_sort Gelu C. Rosianu
title Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma
title_short Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma
title_full Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma
title_fullStr Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma
title_full_unstemmed Endoscopic management of a rare case of obstructive giant duodenal Brunner’s gland hamartoma
title_sort endoscopic management of a rare case of obstructive giant duodenal brunner’s gland hamartoma
publisher Balkan Medical Union
series Archives of the Balkan Medical Union
issn 1584-9244
2558-815X
publishDate 2017-12-01
description Introduction. Brunner’s gland hamartomas are very uncommon. They are small, benign lesions, frequently located in the bulb of the duodenum. Usually found incidentally during routine esophago-gastro-duodenoscopies, these lesions are frequently asymptomatic, but some patients may present with symptoms of duodenal obstruction or hemorrhage secondary to ulceration. Surgical excision is required, especially if the lesion has large dimensions. The pathological examination is the most important in confirming the diagnosis.Case presentation. We report a case of a 64-year-old female patient, who presented to the emergency room for vomiting partially digested food, without blood. Upper digestive endoscopy revealed a polypoid mass, with a 1 cm stalk, located in the duodenal bulb. The polyp was successfully endoscopically resected and the pathological diagnosis was of Brunner’s gland hamartoma. Histologically, this polyp consisted of the components of Brunner’s gland cells, as well as glandular, adipose and muscle cells. Conclusions. Brunner’s gland hamartomas are rare duodenal tumors occurring in middle-aged patients that present either with gastrointestinal hemorrhage, obstructive symptoms or as an incidental finding. Surgical or endoscopic excision is uncomplicated, and the long-term outcome is favorable. The particularity of our case is given by the fact that this lesion was very large, it caused symptoms such as vomiting and was managed solely by endoscopic resection.
topic giant hamartoma
Brunner's gland
endoscopic resection
url http://umbalk.org/wp-content/uploads/2017/12/14.ENDOSCOPIC-MANAGEMENT-OF-A-RARE-CASE.pdf
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