Brunneroma presenting with radiological features of duodeno-duodenal intussusception

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Brunneroma presenting with radiological features of duodeno-duodenal intussusception

Benign tumours of the duodenum are exceedingly rare (incidence <0.01). Approximately 11% of these are Brunner's gland adenoma/Brunneroma or polypoidal hamartoma which is a benign, proliferative lesion of the submucosal Brunner's glands [1]. Duodenoduodenal intussusception (DDI) is a rare presentation of such a tumour with only a few cases reported thus far. We present a case of a large Brunnero...

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Brunneroma: A Rare Cause of Duodeno-duodenal Intussusception

Brunner gland hamartoma (brunneroma) is a rare benign tumor of the duodenum. It is usually asymptomatic and detected incidentally by endoscopy or other imaging modality. The definitive diagnosis is based on histopathological findings. These may mimic tumors of other natures, such as gastrointestinal stromal tumors (GIST), carcinoids, lipomas, and leiomyomas. Here, we present a case of duodenal ...

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Unusual Presentation of Duodenal Ulcer Presenting with Duodenal Intussusception

We present a unique case of duodeno-duodenal intussusception from a duodenal bulb ulcer. A 38-year-old man presented with nausea, vomiting, and abdominal pain. Computed tomography showed duodenal intussusception. Esophagogastroduodenoscopy (EGD) showed a linear gastric ulcer and a duodenal bulb ulcer with an overlying blood clot. Helicobacter pylori status was positive. Intussusception resolved...

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Wilson’s disease presenting with unusual radiological features

Wilson’s disease (WD) is an inherited disorder of copper metabolism. It results in copper deposition in toxic concentrations in liver, brain, eye, etc. Radiological features in the form of extensive gray and white matter abnormalities are rare. Here we report a case of WD presenting with encephalopathy and unusual radiological features. A 26-year-old male, born out of nonconsanguineous marriage...

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ژورنال

عنوان ژورنال: Sri Lanka Journal of Surgery

سال: 2012

ISSN: 2279-2201,1391-491X

DOI: 10.4038/sljs.v30i1.4507