Prenatally diagnosed congenital pyloric atresia in consecutive three siblings: a case report

Peculiar type 1 congenital pyloric atresia: a case report

Pyloric atresia (PA) is a very rare condition. Its incidence is approximately 1 in 100,000 newborns and constitutes about 1% of all intestinal atresias. We describe the neonatal course of a peculiar case of type 1 pyloric atresia, in which the pyloric membrane was connected to a second duodenal membrane through a virtual duodenal lumen in a premature newborn. The atypical variant required an un...

Pyloric atresia: a case report.

Infantile hypertrophic pyloric stenosis (IHPS) is a common cause of gastric outlet obstruction in infant. The prevalence of IHPS ranges from 1.5 to 4.0 in 1000 live birth1. But the incidence of IHPS has been increasing approximately from 1.5 to 4.0 in 1000 live birth to 1:1502. Though pyloric atresia is a very uncommon cause of gastric outlet obstruction in infant but atresia in this region occ...

Congenital Hypertrophic Pyloric Stenosis: A Case Report

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...

Congenital Pyloric Atresia and Associated Anomalies: A Case Series

Congenital pyloric atresia (CPA) is a very rare surgical condition. Eleven patients with the diagnosis of CPA treated at our hospital were retrospectively studied for the age at diagnosis, sex, presenting symptoms, associated anomalies, operative findings, treatment and outcome. Male: Female is 8:3. The age at diagnosis ranged from one day to three years. Associated anomalies were seen in four ...

Congenital pyloric atresia and epidermolysis bullosa.