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A giant Brunner’s gland hamartoma: a rare cause of upper gastrointestinal bleeding

Journal Volume 87 - 2024
Issue Fasc.2 - Letters
Author(s) I. Mendes 1 2, F. Vara-Luiz 1 2, G. Nunes 1 2, J. Cruz 3, S.C. Antunes 4, J. Fonseca 1 2
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PAGES 340-340
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DOI10.51821/87.2.12806
Affiliations:
(1) Gastroenterology Department, Hospital Garcia de Orta, Almada, Portugal
(2) Egas Moniz Center for Interdisciplinary Research (CiiEM), Egas Moniz School of Health and Science, Caparica, Portugal
(3) Radiology Department, Hospital Garcia de Orta, Almada, Portugal
(4) Pathology Department, Hospital Garcia de Orta, Almada, Portugal

A 78-year-old man was admitted with melena, anemia and hypotension. Upper endoscopy revealed a giant lobulated and pedunculated lesion of the duodenal bulb with an ulcerated area (Fig.1A-C). Biopsies performed during upper endoscopy revealed foveolar epithelium with no dysplasia. Abdominal CT showed a nodular lesion protruding to the duodenal lumen with a diameter of approximately 40mm (Fig.2A). Giving the anemia, with recurrent transfusion need, endoscopic resection was proposed. During the intervention an endoloop was deployed at the base of the pedicle and a hot snare polypectomy was successfully performed without complications (Fig.1D). The patient was discharged after the procedure, asymptomatic, with no evidence of bleeding recurrence. Histology (Fig.2B) was consistent with Brunner’s gland hamartoma (BGH).

The authors declare that they have no conflict of interest.
© Acta Gastro-Enterologica Belgica.
PMID 39210769