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      Brunner's Gland Hyperplasia: A Massive Duodenal Lesion

      case-report
      1 , , 2 , 3
      ,
      Cureus
      Cureus
      brunneroma, brunner's gland hyperplasia, iron deficiency anemia, gastric outlet obstruction

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          Abstract

          A 57-year-old male with a history of gastroesophageal reflux disease and esophageal strictures presented with melena and abdominal pain. He underwent an esophagogastroduodenoscopy, which revealed a 5-cm duodenal bulb mass causing partial obstruction of the gastric outlet. Endoscopic ultrasound showed a 5-cm, hypoechoic lesion, arising from the mucosal layer, with a large blood vessel feeding the lesion. Biopsy revealed benign Brunner’s gland hyperplasia. The large mass was causing symptomatic obstruction of the pylorus and iron deficiency anemia, and had risk for malignant transformation. Due to its size it was not amenable to endoscopic removal. Subsequently, he underwent exploratory laparotomy with pyloroplasty, duodenotomy and partial duodenal resection. Surgical pathology showed Brunner’s gland hyperplasia and was negative for malignancy. 

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          Most cited references14

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          Brunner's gland hyperplasia and hamartoma: imaging features with clinicopathologic correlation.

          The purpose of this essay is to describe, illustrate, and correlate the imaging and pathologic features of Brunner's gland hyperplasia and Brunner's gland hamartoma. This article summarizes our experience with pathologically proven cases of Brunner's hyperplasia and hamartoma accessioned into the radiologic pathology archive of the Armed Forces Institute of Pathology.
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            Gastric foveolar metaplasia with dysplastic changes in Brunner gland hyperplasia: possible precursor lesions for Brunner gland adenocarcinoma.

            Cases of adenocarcinomas developed in Brunner gland hyperplasia (BGH) have been sporadically reported. Herein, we report the morphologic spectrum of hyperplastic changes culminating into dysplasia and carcinoma in 722 cases of BGH listed in our files. Fifteen of these cases showed dysplastic changes, with 8 graded as low-grade dysplasia, 5 as high-grade dysplasia, 11 as atypical hyperplasia, and 2 as invasive carcinoma, although each frequently coexisted in the same tumor. In two carcinomas, one had high-grade dysplasia in the mucosa, and another had only atypical hyperplasia. Interestingly, hyperplastic glands around dysplastic foci were associated with gastric foveolar metaplasia and papillary configuration in 13 cases, 11 of which showed a gradual increase in nuclear atypism in the transition from metaplastic to dysplastic glands. All of the metaplastic gastric glands showed diffuse and strong immunopositivity for gastric foveolar mucin (MUC5AC). Immunohistochemical profiles also supported the concept of a continuous spectrum in carcinogenesis from gastric foveolar hyperplasia through atypical hyperplasia or dysplasia and eventually to frank adenocarcinoma. The results of our study suggest, therefore, that dysplastic and/or carcinomatous change does occur in BGH, that they form the continuous morphologic spectrum, and that papillary foveolar metaplasia may be a precursor lesion in the process of carcinogenesis with a background of BGH.
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              Tumors of the small intestine. A review of experience with 115 cases including a report of a rare case of malignant hemangio-endothelioma.

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                Author and article information

                Journal
                Cureus
                Cureus
                2168-8184
                Cureus
                Cureus (Palo Alto (CA) )
                2168-8184
                4 April 2020
                April 2020
                : 12
                : 4
                : e7542
                Affiliations
                [1 ] Internal Medicine, University of Louisville School of Medicine, Louisville, USA
                [2 ] Pathology, University of Louisville School of Medicine, Louisville, USA
                [3 ] Gastroenterology, University of Louisville, Louisville, USA
                Author notes
                Article
                10.7759/cureus.7542
                7198079
                8eff1c97-0f48-483c-ab26-586f7cb608e5
                Copyright © 2020, Bhatti et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 28 February 2020
                : 3 April 2020
                Categories
                Internal Medicine
                Gastroenterology
                General Surgery

                brunneroma,brunner's gland hyperplasia,iron deficiency anemia,gastric outlet obstruction

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