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CASE REPORT |
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Year : 2006 | Volume
: 52
| Issue : 1 | Page : 38-40 |
Brunner's gland hyperplasia at the ampulla of Vater
SE J Janes1, AM Zaitoun2, JA Catton1, GP Aithal3, IJ Beckingham1
1 Departments of Surgery, Queens Medical Centre, Nottingham, United Kingdom 2 Departments of Histopathology, Queens Medical Centre, Nottingham, United Kingdom 3 Departments of Gastroenterology, Queens Medical Centre, Nottingham, United Kingdom
Correspondence Address:
SE J Janes Departments of Surgery, Queens Medical Centre, Nottingham United Kingdom
 Source of Support: None, Conflict of Interest: None  | Check |
PMID: 16534163 
Brunner's gland hyperplasia (BGH) is a diagnostic challenge where in the pathophysiology and natural history remain poorly understood. This Case Report describes BGH arising at the ampulla of Vater, causing abdominal pain and vomiting in a 46-year-old man. Owing to the inconclusive nature of imaging studies and suspicious intraoperative findings, a Whipple resection was performed without any complications. Histological analysis showed that the obstructing lesion was BGH, with no evidence of malignancy. This is only the second such case of its kind at the ampulla of Vater to be reported. In addition, we present the previously unreported endoscopic ultrasound findings. The subsequent literature review focuses on the pathophysiology, clinical presentation, diagnosis, and management of BGH.
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