Pyloric stenosis is a narrowing of the pylorus, the opening of the stomach into the small intestine.
Pyloric stenosis is caused by a thickening of the muscles of the pylorus. This thickening prevents the stomach from emptying into the small intestine.
The cause of the thickening is unknown, although genetic factors may play a role. Pyloric stenosis occurs more commonly in boys than in girls, and is rare in patients older than 6 months. The condition is usually diagnosed by the time a child is 6 months old.
Symptoms generally appear several weeks after birth:
Physical examination may show signs of dehydration. The infant may have a distended abdomen. Palpation of the abdomen may reveal the abnormal pylorus, which feels like an olive-shaped mass.
Treatment for pyloric stenosis involves surgery (Ramstedt pyloromyotomy) to split the overdeveloped muscles of the pylorus.
Balloon dilation is less effective, but may be considered for infants when the risk of general anesthesia is high.
The patient will be given intravenous fluids, usually prior to surgery.
Surgical repair usually provides complete relief of symptoms.
Small, frequent feedings are usually well tolerated several hours after the surgery.
Call your health care provider if symptoms suggestive of pyloric stenosis develop in your infant.