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Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report

Brunner’s gland hamartoma is a rare benign tumour of the duodenum. It was first described by Cruveilhier in 1835. Presently around 200 cases have been reported in literature. No sex predilection is seen. Patients usually present in the fifth to sixth decades of life. They may be clinically silent or...

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Autores principales: Sen, Rajeev, Gupta, Veena, Sharma, Nisha, Chawla, Nitika, Kumar, Sanjay, Malik, Shivani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Association of Gastroerterology and Hepatology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208932/
https://www.ncbi.nlm.nih.gov/pubmed/25349687
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author Sen, Rajeev
Gupta, Veena
Sharma, Nisha
Chawla, Nitika
Kumar, Sanjay
Malik, Shivani
author_facet Sen, Rajeev
Gupta, Veena
Sharma, Nisha
Chawla, Nitika
Kumar, Sanjay
Malik, Shivani
author_sort Sen, Rajeev
collection PubMed
description Brunner’s gland hamartoma is a rare benign tumour of the duodenum. It was first described by Cruveilhier in 1835. Presently around 200 cases have been reported in literature. No sex predilection is seen. Patients usually present in the fifth to sixth decades of life. They may be clinically silent or may present with variable symptoms and occasionally obstructive symptoms and chronic pancreatitis. Endoscopic presentation can be nodular, polypoid or diffuse glandular proliferation with thickening of duodenal wall and hence can be misdiagnosed as malignancy. We describe a case of duodenal tumor reported outside (on biopsy) as well differentiated adenocarcinoma which out as Brunner gland hamartoma upon complete resection. Brunner gland hamartoma may sometimes have a very unusual presentation. Extensive pre-operative evaluation is necessity to avoid radical surgical procedure.
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spelling pubmed-42089322014-10-27 Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report Sen, Rajeev Gupta, Veena Sharma, Nisha Chawla, Nitika Kumar, Sanjay Malik, Shivani Middle East J Dig Dis Case Report Brunner’s gland hamartoma is a rare benign tumour of the duodenum. It was first described by Cruveilhier in 1835. Presently around 200 cases have been reported in literature. No sex predilection is seen. Patients usually present in the fifth to sixth decades of life. They may be clinically silent or may present with variable symptoms and occasionally obstructive symptoms and chronic pancreatitis. Endoscopic presentation can be nodular, polypoid or diffuse glandular proliferation with thickening of duodenal wall and hence can be misdiagnosed as malignancy. We describe a case of duodenal tumor reported outside (on biopsy) as well differentiated adenocarcinoma which out as Brunner gland hamartoma upon complete resection. Brunner gland hamartoma may sometimes have a very unusual presentation. Extensive pre-operative evaluation is necessity to avoid radical surgical procedure. Iranian Association of Gastroerterology and Hepatology 2014-10 /pmc/articles/PMC4208932/ /pubmed/25349687 Text en © 2014 by Middle East Journal of Digestive Diseases This work is published by Middle East Journal of Digestive Diseases as an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-sa/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Case Report
Sen, Rajeev
Gupta, Veena
Sharma, Nisha
Chawla, Nitika
Kumar, Sanjay
Malik, Shivani
Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report
title Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report
title_full Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report
title_fullStr Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report
title_full_unstemmed Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report
title_short Brunner Gland Hamartoma Masquerading as Malignancy; A Rare Case Report
title_sort brunner gland hamartoma masquerading as malignancy; a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208932/
https://www.ncbi.nlm.nih.gov/pubmed/25349687
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