Yuan XY, Huang YQ. Congenital double pylorus with duodenal ulcer: A case report and review of the literature.
Shijie Huaren Xiaohua Zazhi 2016;
24:4024-4028. [DOI:
10.11569/wcjd.v24.i28.4024]
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Abstract
Congenital double pylorus (CDP) is an extremely rare congenital disease in which both the prosopyle and apopyle are intercommunicated with the gastric antrum and duodenal bulb. The pylorus of CDP is composed of normal mucous epithelium, the lamina propria, and the muscularis mucosae. However, a few CDP operations have proved the lack of the muscularis mucosae but the existence of heterotopic pancreas tissues in the pylorus of CDP. This article reports a case of CDP complicated with duodenal ulcer in a 67-year-old man. He presented with repeated epigastric pain for 8 years and melena for 6 years, with recurrence for 3 d. He was positive for Helicobacter pylori (H. pylori) antibody. Gastroendoscopy performed 8 years ago revealed double pylorus, bile reflux gastritis, and duodenal bulbar inflammation. Gastroendoscopy performed 6 years ago revealed double pylorus with a duodenal bulbar ulcer lesion, and pathological examination suggested chronic inflammation in the duodenal bulbar mucosa, accompanied with low grade gland dysplasia. A second gastroendoscopy performed 6 years ago also revealed double pylorus with a duodenal bulbar ulcer (A2 stage). Gastroendoscopy at our hospital revealed double pylorus and pyloric canal inflammation, and pathological examination suggested pyloric canal mucosal inflammation accompanied with erosion and mild intestinal metaplasia. He was then given proton pump inhibitor therapy combined with anti-H. pylori therapy, and his symptoms were obviously improved. This case suggests that gastroendoscopy is the most direct and accurate method for the diagnosis of CDP.
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