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A Case of Double Duodenal Web Associated with Peptic Ulcer

Journal of the Korean Pediatric Society 1997;40(9):1319-1324.
Published online September 15, 1997.
A Case of Double Duodenal Web Associated with Peptic Ulcer
Sun Young Park, Jin Hwa Jung, Jeong Ho Lee, Jong Dae Jo
Department of Pediatrics, Maryknoll Hospital, Pusan, Korea
소화성 궤양을 동반한 십이지장 이중 격막(Double Duodenal W eb) 1례
박선영, 정진화, 이정호, 조종대
부산 메리놀병원 소아과
Abstract
Duodenal web is a very rare congenital anomaly which usually causes clinical features of intestinal obstruction from early infancy. It shows characteristic findings in the radiologic contrast study or endoscopy. But in the cases with large openings, preoperative diagnosis of web is difficult and often is overlooked until adolescence or adulthood because of delayed onset of symptoms. Duodenal web is usually single near the ampulla of Vater and may be multiple. Only a few cases of double duodenal webs have been reported in the literature. We experienced a case of double duodenal web in a 15 year-old girl who complained of peptic ulcer-associated symptoms including epigastric pain and bloody stool. She had suffered from longstanding abdominal symptoms, malnutrition and iron-deficiency anemia. We propose that duodenal web should be kept in mind for patients with a history of chronic gastrointestinal obstructive symptoms and atypical peptic ulcer.
Key Words: Duodenal web, Peptic ulcer


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