Adult hypertrophic pyloric stenosis that improved by spontaneous double channel pylorus formation
JGH Open, Volume 5, Issue 2, Page 317-319, February 2021., 2021 This article presents an adult‐onset case of hypertrophic pyloric stenosis (AHPS). In this case, long term (over six months) persisting thickening of the muscularis propria in the pyloric region proved the precise diagnosis of AHPS. Furthermore, it is very interesting that double pylorus due to possible penetrating gastric ulcer led to the improvement ...
Aiji Hattori +6 more
wiley +1 more source
The Turkish Journal of Pediatrics, 1999 Although infantile hypertrophic pyloric stenosis following esophageal atresia repair is known, infantile hypertrophic pyloric stenosis following H-type tracheoesophageal fistula has not been encountered previously.
Pelin Oğuzkurt +3 more
doaj +1 more source
Role of Ultrasonography in the Diagnosis of Infantile Hypertrophic Pyloric Stenosis [PDF]
Journal of Clinical and Diagnostic Research, 2023 A 28-day-old male baby was brought by his mother with complaints of projectile non-bilious vomitings after feeds, excessive crying, and decreased frequency of stools for three days.
Prasanthi Ramesh Ghanta +4 more
doaj +1 more source
Gastric outlet obstruction in an 11-year-old girl: A case report. [PDF]
JPGN RepAbstract Pyloric stenosis commonly affects infants and rarely causes gastric outlet obstruction in adolescents and older children. We present the case of an 11‐year‐old girl with a 2‐month history of recurrent postprandial vomiting and weight loss. On physical examination, the patient presented with abdominal distension.
Figueiredo AS +7 more
europepmc +2 more sources
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report [PDF]
, 2022 Background: Contiguous gene deletion syndrome at Xp22.3 resulting in nullisomy in males or Turner syndrome patients typically encompasses the steroid sulfatase gene (STS) and contiguously located other genes expanding the phenotype.
Antona V. +8 more
core +1 more source
Infantile hypertrophic pyloric stenosis in monozygotic twins: a case report and review of genetic and modifiable risk factors [PDF]
, 2018 Infantile hypertrophic pyloric stenosis is the most common surgical pathology resulting in emesis presenting in infancy and is usually encountered between the second and eighth weeks of life.
Baker, Dustin +3 more
core +2 more sources
Duodenal pancreatic heterotopia causing acute pancreatitis with gastric outlet obstruction
, 2022 ANZ Journal of Surgery, Volume 92, Issue 11, Page 3078-3079, November 2022.
William Fleischl +4 more
wiley +1 more source
Our experience of laparoscopic pyloromyotomy with ultrasound-guided parameters
Journal of Minimal Access Surgery, 2019 Traditional management of infantile Hypertrophic Pyloric Stenosis is open pyloromyotomy after initial adequate resuscitation of the patient. From 1991, laparoscopic approach is considered feasible and safe.
Aboli Hukeri +7 more
doaj +1 more source
Infantile Hypertrophic Pyloric Stenosis [PDF]
Yeungnam University Journal of Medicine, 1996 Infantile hypertrophic pyloric stenosis(IHPS), which occurs three of 1,000 live births, is a major cause of nonbilious vomiting of early infancy but its etiology and pathogenesis are still obscure. The operation of pyloromyotomy as described by Ramstedt in 1912 remains the standard of care for the treatment of IHPS.
Young Soo Huh +2 more
openaire +2 more sources
Infantile Hypertrophic Pyloric Stenosis [PDF]
, 2020 In hypertrophic pyloric stenosis, there is a functional obstruction at the gastric outlet as a result of hypertrophy and hyperplasia of the muscular layers of the pylorus. It is a common cause of gastric outlet obstruction and surgical vomiting in infants. Infants typically present with forceful nonbilious vomiting mostly shortly after feeds. Prolonged
Emmanuel A. Ameh +2 more
openaire +1 more source