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Pyloric stenosis - infant

Congenital hypertrophic pyloric stenosis; Infantile hypertrophic pyloric stenosis; Gastric outlet obstruction

 

Pyloric stenosis is a narrowing of the pylorus, the opening from the stomach into the small intestine. This article describes the condition in infants.

Causes

 

Normally, food passes easily from the stomach into the first part of the small intestine through a valve called the pylorus. With pyloric stenosis, the muscles of the pylorus are thickened. This prevents the stomach from emptying into the small intestine.

The exact cause of the thickening is unknown. Genes may play a role, since children of parents who had pyloric stenosis are more likely to have this condition. Other risk factors include certain antibiotics, too much acid in the first part of the small intestine (duodenum), and certain diseases a baby is born with, such as diabetes.

Pyloric stenosis occurs most often in infants younger than 6 months. It is more common in boys than in girls.

 

Symptoms

 

Vomiting is the first symptom in most children:

  • Vomiting may occur after every feeding or only after some feedings
  • Vomiting usually starts around 3 weeks of age, but may start any time between 1 week and 5 months of age
  • Vomiting is forceful (projectile vomiting)
  • The infant is hungry after vomiting and wants to feed again

Other symptoms appear several weeks after birth and may include:

  • Abdominal pain
  • Burping
  • Constant hunger
  • Dehydration (gets worse as vomiting gets worse)
  • Failure to gain weight or weight loss
  • Wave-like motion of the abdomen shortly after feeding and just before vomiting occurs

 

Exams and Tests

 

The condition is usually diagnosed before the baby is 6 months old.

A physical exam may reveal:

  • Signs of dehydration, such as dry skin and mouth, less tearing when crying, and dry diapers
  • Swollen belly
  • Olive-shaped mass when feeling the upper belly, which is the abnormal pylorus

Ultrasound of the abdomen may be the first imaging test. Other tests that may be done include:

  • Barium x-ray -- reveals a swollen stomach and narrowed pylorus
  • Blood tests -- often reveals an electrolyte imbalance

 

Treatment

 

Treatment for pyloric stenosis involves surgery to widen the pylorus. The surgery is called pyloromyotomy.

If putting the infant to sleep for surgery is not safe, a device called an endoscope with a tiny balloon at the end is used. The balloon is inflated to widen the pylorus.

In infants who cannot have surgery, tube feeding or medicine to relax the pylorus is tried.

 

Outlook (Prognosis)

 

Surgery usually relieves all symptoms. As soon as several hours after surgery, the infant can start small, frequent feedings.

 

Possible Complications

 

If pyloric stenosis isn't treated, a baby won't get enough nutrition and fluid, and can become underweight and dehydrated.

 

When to Contact a Medical Professional

 

Call your health care provider if your baby has symptoms of this condition.

 

 

References

Hunter AK, Liacouras CA. Pyloric stenosis and other congenital anomalies of the stomach. In: Kliegman RM, Stanton BF, St. Geme, Schor NF, eds. Nelson Textbook of Pediatrics . 20th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 329.

Kanters A, Ponsky T. Pyloromyotomy for pyloric stenosis. In: Delaney CP, ed. Netter's Surgical Anatomy and Approaches . Philadelphia, PA: Elsevier Saunders; 2014:chap 10.

 
  • Digestive system - illustration

    The esophagus, stomach, large and small intestine, aided by the liver, gallbladder and pancreas convert the nutritive components of food into energy and break down the non-nutritive components into waste to be excreted.

    Digestive system

    illustration

  • Pyloric stenosis - illustration

    A narrowing of the outlet from the stomach to the small intestine (called the pylorus) that occurs in infants.

    Pyloric stenosis

    illustration

  • Pyloric stenosis - infant - Series

    Presentation

  •  
    • Digestive system - illustration

      The esophagus, stomach, large and small intestine, aided by the liver, gallbladder and pancreas convert the nutritive components of food into energy and break down the non-nutritive components into waste to be excreted.

      Digestive system

      illustration

    • Pyloric stenosis - illustration

      A narrowing of the outlet from the stomach to the small intestine (called the pylorus) that occurs in infants.

      Pyloric stenosis

      illustration

    • Pyloric stenosis - infant - Series

      Presentation

    •  

    Self Care

     

      Tests for Pyloric stenosis - infant

       

         

        Review Date: 7/10/2015

        Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.

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