Congenital Hypertrophic Pyloric Stenosis: A Case Report | ||
Journal of Pediatric Perspectives | ||
مقاله 9، دوره 8، شماره 6 - شماره پیاپی 78، شهریور 2020، صفحه 11467-11471 اصل مقاله (384.94 K) | ||
شناسه دیجیتال (DOI): 10.22038/ijp.2019.44013.3654 | ||
نویسندگان | ||
Mehdi Foroughi1؛ Zahra Beizavi* 2؛ Razieh Sadat Mousavi-Roknabadi3 | ||
1MD, Pediatric Surgery Specialist, Department of Pediatric Surgery, Namazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran. | ||
2MD, General Surgery Specialist, Department of General Surgery, Shiraz University of Medical Sciences, Shiraz, Iran. | ||
3MD, Community Medicine Specialist, Emergency Medicine Department, Shiraz University of Medical Sciences, Shiraz, Iran. | ||
چکیده | ||
Background Hypertrophic pyloric stenosis (HPS) is a common surgical condition in infancy, and typically presents at 2-4 weeks of age. Case Presentation A full term male neonate in Zeinabieh hospital, Shiraz, Iran was presented with oral feeding intolerance from birth, bile-stained output of nasogastric tube, and a double bubble sign on abdominal radiography suspected to duodenal atresia. However subsequent laparotomy on 3rd day of life revealed HPS. Conclusion This condition should be considered as part of a rare differential diagnosis of newborn with sign of obstruction at birth. | ||
کلیدواژهها | ||
Congenital؛ Hypertrophic Pyloric Stenosis؛ Newborn | ||
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