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A Case of Congenitial Pyloric Atresia

Journal of the Korean Pediatric Society 1995;38(12):1713-1717.
Published online December 15, 1995.
A Case of Congenitial Pyloric Atresia
Hyeon Jeong Lee1, Jun Hoe1, Jeong Hwa Whang1, Gae Soon Yeo1, Hee Jin Kim1, Chan Yung Kim1, Jun Hyeon Kim2
1Department of Pediatrics, Choon Hae Hospital, Pusan, Korea
2Department of General Surgery, Choon Hae Hospital, Pusan, Korea
선천성 유문 폐쇄증 1례
이현정1, 허준1, 황정화1, 여계순1, 김희진1, 김찬영1, 김준현2
1춘해병원 소아과
2춘해병원 일반외과
Abstract
In the newborn, a complete occlusion of the pyloric outlet is an extremely rare event. Authors experienced a case of pyloric atresia in a 2-day old boy, Who was admitted because of nonbilious vomiting. The plain radiograph of the abdomen showed gas in the huge stomach, but no gas noted distally. At operation, 3 days after birth, the pylorus was atretic with a gap of 3mm between stomach and duodenum, and gastroduodenostomy was carried out. Follow up UGI series revealed satisfactory gastrodeodenal anastomosis and gastric emptying. The baby was discharged on the tenth postoperative day and appeared healthy and normal in every respect. The brief review of related literatures was also made.
Key Words: Congenital pyloric atresia


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