Postoperative courses were uneventful in 87.4% of cases. All the infants were treated surgically unless three patients dying before operation, because of a late diagnosis. The diagnosis was confirmed by ultrasonography and sometimes contrast upper gastrointestinal study. The classical symptom of projectile vomiting was always present, a pyloric tumor was palpated in 19.7% of the cases, metabolic disturbance was noted in 44.3% of patients. In this study male sex was predominant, with a sex-ratio of 3.8/1.

We conducted a retrospective review of 142 patients presenting HPS, between 19. Analysis of our results and comparison with literature to determine particularities of HPS in our country.

Hypertrophic pyloric stenosis (HPS) is a common condition affecting infants before the first three months of life. Jlidi, Said Ben Youssef, Dhouha Ghorbel, Sofiene Mattoussi, Nadia Khemakhem, Rachid Nouira, Faouzi Chaouachi, BÃ©ji Imaging tests, fundamentally magnetic resonance imaging, were very important in the characterization and diagnosis of this entity. We present a case of a pyloric adenomyoma that clinically simulated hypertrophic pyloric stenosis in a newborn girl. On histologic examination, these tumors have an epithelial component similar to pancreatic ducts. Gastric adenomyomas are extremely uncommon benign tumors in children. SÃ¡nchez GarcÃa, S Rubio SolÃs, D Anes GonzÃ¡lez, G GonzÃ¡lez SÃ¡nchez, S This article reviews the literature on pyloric duplications and describes a pyloric duplication associated with hypertrophic pyloric stenosis in a 5-week-old child and a duplication that recurred 7 years later. Pyloric duplications are particularly rare few are reported in the English literature. Gastric duplications are unusual congenital anomalies that often require surgical treatment. Pyloric duplications: review and case study. The operative procedure herein described is essentially that devised by Ramstedt many years ago, with modifications to facilitate the procedure. The position of the tumor governs the choice between two different incisions. Preparation for operation consists of intravenous administration of fluids and electrolytes and sometimes serum or whole blood. Pylorotomy for treatment of hypertrophic pyloric stenosis was not successful until the development of necessary supporting measures.

Roentgenological studies are rarely indicated. The diagnosis is made by a history of projectile vomiting and failure to gain weight, the observation of gastric peristaltic waves, and the palpation of a pyloric â€œtumor.â€ A method of palpating this tumor is described in detail. Hypertrophic pyloric stenosis, a relatively common condition, is caused by hyperplasia of the musculature of the pylorus. The patterns of associated anomalies with penile agenesis, and those of congenital hypertrophic pyloric stenosis are discussed. Yagmurlu, Aydin Vargun, Rahsan Gollu, Gulnur Gokcora, I HalukĪ neonate with penile agenesis and congenital hypertrophic pyloric stenosis is presented. Penile agenesis and congenital hypertrophic pyloric stenosis: an association or a random coexistence?

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