Pyloric stenosis is a narrowing of the opening from the stomach to the first part of the small intestine, the pylorus. Symptoms include projectile vomiting without bile, most often after feeding, and typically become obvious at two to twelve weeks of age. The cause is unclear; risk factors in babies include birth by cesarean section, preterm birth, bottle feeding and being firstborn. It is diagnosed by feeling an olive-shaped mass in the abdomen, often confirmed by ultrasound. Treatment starts by correcting dehydration and electrolyte problems and is typically followed by surgery, first carried out in 1912 by Conrad Ramstedt. About one to two per 1,000 babies are affected, males about four times more often than females.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category)Idiopathic / Multifactorial 1 First Described Pyloric Stenosis
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Source Pyloromyotomy (Wikipedia)
Sources
1. Wikipedia: Pyloric stenosis
Lead
Pyloric stenosis is a narrowing of the opening from the stomach to the first part of the small intestine (the pylorus).
Lead (causative-agent-category)
The cause of pyloric stenosis is unclear.
Lead (first-described-year)
The first description of pyloric stenosis was in 1888, with surgical management first carried out in 1912 by Conrad Ramstedt.
View the Source2. World Health Organization: ICD-10 Version:2019 - Q38-Q45 Other congenital malformations of the digestive system
World Health OrganizationICD-10 2019 category Q40.0, Chapter XVIIQuote, ICD-10 2019 category Q40.0, Chapter XVII
Q40.0 Congenital hypertrophic pyloric stenosis
View the Source Pyloromyotomy (Wikipedia)
Wikimedia FoundationTreated By: Pyloromyotomy, Lead (695566)Quote, Treated By: Pyloromyotomy, Lead (695566)
The procedure is typically performed in cases of "hypertrophic pyloric stenosis" in young children.
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