Hirschsprung (HIRSH-sproong) disease is a condition in which nerve cells are missing in a baby's large intestine, resulting in bowel blockage. These nerve cells help move contents through the colon. Without them, the contents can back up and cause problems with passing stool. Hirschsprung disease is present at birth.
A newborn who has Hirschsprung disease usually can't have a bowel movement in the days after birth. In mild cases, there might not be symptoms until later in childhood. Rarely, Hirschsprung disease is first diagnosed in adults.
The treatment is surgery to bypass or remove the affected part of the colon.
Symptoms of Hirschsprung disease depend on how bad the condition is. Usually symptoms start shortly after birth, but sometimes don't show up until later in life.
Typically, the most obvious symptom is a newborn's failure to have a bowel movement within 48 hours after birth.
Other symptoms in newborns may include:
In older children, symptoms can include:
The cause of Hirschsprung disease is unclear. It sometimes runs in families. In some cases, it might be associated with an altered gene.
Hirschsprung disease occurs when nerve cells in the colon don't develop all the way. Nerves in the colon control the muscle contractions that move food through the bowels. Without the contractions, stool stays in the large intestine.
Factors that may increase the risk of Hirschsprung disease include:
Children who have Hirschsprung disease could develop enterocolitis, a serious intestinal infection. Enterocolitis can be life-threatening and should be treated right away.
To diagnose Hirschsprung disease, a healthcare professional will do an exam and ask questions about the child's bowel movements. One or more of the following tests may be recommended to diagnose or rule out Hirschsprung disease:
Stomach X-ray using a contrast dye. A dye is placed into the bowel through a special tube placed in the rectum. The dye fills and coats the lining of the bowel, showing a clear outline of the colon and rectum.
The X-ray will often show the difference between the part of bowel without nerves and the often-swollen section of bowel behind it.
Hirschsprung disease is typically treated with surgery to bypass or remove the part of the colon that's missing nerve cells. There are two ways this can be done: a pull-through surgery or an ostomy surgery.
In this procedure, the lining of the diseased part of the colon is stripped away. Then, the healthy section is pulled through the colon from the inside and attached to the anus. This is usually done using minimally invasive methods, operating through the anus.
In children who are very ill, surgery might be done in two steps.
First, the diseased part of the colon is removed. The healthy part of the colon is then connected to an opening created in the child's belly, called a stoma. Stool leaves the body through the opening into a bag. The bag attaches to the end of the intestine that comes through the stoma. This allows time for the lower part of the colon to heal.
Once the colon has had time to heal, a second procedure is done to close the stoma and connect the healthy part of the intestine to the rectum or anus.
After surgery, most children can pass stool through the anus.
Possible complications that may improve with time include:
Children also continue to be at risk of developing enterocolitis after surgery, especially in the first year. Call a healthcare professional right away if any of the symptoms of enterocolitis occur, such as:
If your child has constipation after surgery for Hirschsprung disease, talk with a healthcare professional about whether you should:
Serve high-fiber foods. If your child eats solid foods, include high-fiber foods. Offer whole grains, fruits and vegetables and limit white bread and other low-fiber foods. A sudden increase in high-fiber foods can worsen constipation at first, so add high-fiber foods to your child's diet slowly.
If your child isn't eating solid foods yet, ask the health professional about formulas that might help relieve constipation. Some infants might need a feeding tube for a while.
Hirschsprung disease is often diagnosed in the hospital shortly after birth, or symptoms of the condition show up later. If your child has symptoms that worry you, especially constipation and a swollen abdomen, talk to a healthcare professional.
You might be referred to a digestive disorders specialist, called a gastroenterologist, or to the emergency department if your child's symptoms are severe.
Here's some information to help you get ready for your appointment.
When you make the appointment, ask if there's anything your child needs to do in advance, such as fasting for a specific test. Make a list of:
Take a family member or friend along, if possible, to help you remember the information you're given.
For Hirschsprung disease, basic questions to ask include:
Don't hesitate to ask other questions.
You're likely to be asked a few questions, including: