Congenital Hypertrophic Pyloric Stenosis: A Case Report

Foroughi, Mehdi; Beizavi, Zahra; Mousavi-Roknabadi, Razieh Sadat

doi:10.22038/ijp.2019.44013.3654

Congenital Hypertrophic Pyloric Stenosis: A Case Report

Authors

Mehdi Foroughi ¹

Zahra Beizavi ²

Razieh Sadat Mousavi-Roknabadi ³

¹ MD, Pediatric Surgery Specialist, Department of Pediatric Surgery, Namazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.

² MD, General Surgery Specialist, Department of General Surgery, Shiraz University of Medical Sciences, Shiraz, Iran.

³ MD, Community Medicine Specialist, Emergency Medicine Department, Shiraz University of Medical Sciences, Shiraz, Iran.

10.22038/ijp.2019.44013.3654

Abstract

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 3^rd 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.

Keywords

Congenital

Hypertrophic Pyloric Stenosis

Newborn