Pyloric stenosis is a condition that affects infants, typically occurring within the first few weeks after birth. It involves an abnormal narrowing of the pylorus, which is the muscular valve that separates the stomach from the small intestine. This narrowing restricts the passage of food from the stomach into the intestines, leading to symptoms such as frequent vomiting and poor weight gain.
The exact cause of pyloric stenosis is not known. It is believed to be a combination of genetic and environmental factors. It is more commonly seen in males and can sometimes run in families.
The primary symptom of pyloric stenosis is projectile vomiting, which typically occurs shortly after feeding. The vomit may be forceful and may contain partially digested milk. Other symptoms include a swollen or firm abdomen, constant hunger despite frequent feeding, and fewer wet diapers.
Pyloric stenosis is typically diagnosed through a thorough physical examination and medical history review. Ultrasound imaging may be used to confirm the diagnosis by showing the thickness and length of the narrowed pyloric muscle.
The primary treatment for pyloric stenosis is surgery, known as a pyloromyotomy. During this procedure, a small incision is made in the pyloric muscle to relieve the narrowing and allow for proper food passage. The surgery is minimally invasive and has a high success rate.
After the surgery, infants usually experience a rapid improvement in symptoms. Feeding can typically resume within a few hours after the procedure, and most infants can be discharged from the hospital within a day or two. Regular follow-up appointments will be scheduled to monitor the infant’s progress.