Hirschsprung's disease (patient information): Difference between revisions
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The abnormal section of colon must be surgically removed. Sometimes this can be done in one operation. However, it is frequently done in two parts with a colostomy being performed first, and another procedure being performed later in the first year of life. | The abnormal section of colon must be surgically removed. Sometimes this can be done in one operation. However, it is frequently done in two parts with a colostomy being performed first, and another procedure being performed later in the first year of life. | ||
==Diseases with similar symptoms== | ==Diseases with similar symptoms== | ||
* | *[[Intestinal cyst]] or [[tumor]] | ||
* | *[[Meconium plug syndrome]] | ||
==Where to find medical care for Hirschsprung's disease== | ==Where to find medical care for Hirschsprung's disease== | ||
Revision as of 19:54, 3 March 2010
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What is Hirschsprung's disease?
Hirschsprung's disease is a blockage of the large intestine due to improper muscle movement in the bowel. It is a congenital condition, which means it is present from birth.
What are the symptoms of Hirschsprung's disease?
- Constipation
- Failure to pass meconium shortly after birth
- Failure to pass a first stool within 24 - 48 hours after birth
- Malabsorption
- Poor weight gain
- Slow growth (child 0-5 years)
- Swollen belly
- Vomiting
- Watery diarrhea (in the newborn)
What are the causes of Hirschsprung's disease?
Muscle contractions in the gut help digested materials move through the intestine. This is called peristalsis. Nerves in between the muscle layers trigger the contractions.
In Hirschsprung's disease, the nerves are missing from a short or long part of the bowel. Areas without such nerves can not push material through. This causes a blockage. Intestinal contents build up behind the blockage, causing the bowel and abdomen to become swollen. If the condition is severe, the newborn may fail to pass meconium or stool, and the newborn may vomit.
Milder cases may not be diagnosed until a later age. In older children, the disease may be cause chronic constipation, abdominal swelling, and decreased growth.
Hirschsprung's disease causes about 25% of all newborn intestinal obstruction. It occurs five times more frequently in males than in females. Hirschsprung's disease is sometimes associated with other inherited or congenital conditions such as Down syndrome.
Who is at risk for Hirschsprung's disease?
Risk Factors include:
- gender: males have a higher risk than females
- having a congenital condition such as Down Syndrome
How to know you have Hirschsprung's disease?
During a physical examination, the doctor may be able to feel loops of bowel in the swollen belly. A rectal examination may reveal a loss of muscle tone in the rectal muscles.
Tests used to help diagnose Hirschsprung's disease may include:
- Abdominal x-ray
- Anal manometry (a balloon is inflated in the rectum to measure pressure in the area)
- Barium enema
- Rectal biopsy
When to seek urgent medical care
Call your child's health care provider if symptoms of Hirschsprung's disease develop.
Call your child's health care provider if your child has abdominal pain or other new symptoms after being treated for this condition.
Treatment options
The abnormal section of colon must be surgically removed. Sometimes this can be done in one operation. However, it is frequently done in two parts with a colostomy being performed first, and another procedure being performed later in the first year of life.
Diseases with similar symptoms
Where to find medical care for Hirschsprung's disease
Directions to Hospitals Treating Hirschsprung's disease
What to expect (Outlook/Prognosis)
Symptoms improve or are eliminated in most children after surgical treatment. A better outcome is associated with early treatment and shorter bowel segment involvement.
Possible Complications
- Inflammation and infection of the intestines (enterocolitis)
- Perforation of the intestine
- Short bowel syndrome, a condition that can lead to malnourishment and dehydration
Sources