About Megacolon (Hirschsprung Disease)
Learn about the disease, illness and/or condition Megacolon (Hirschsprung Disease) including: symptoms, causes, treatments, contraindications and conditions at ClusterMed.info.
Megacolon (Hirschsprung Disease)
Megacolon (Hirschsprung Disease) |
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Megacolon (Hirschsprung Disease) InformationHirschsprung disease definition and facts*Medical facts edited by Charles Patrick Davis, MD, PhD
Signs and symptoms in toddlers and older childrenSymptoms of Hirschsprung disease in toddlers and older children may include
Signs and symptoms of Hirschsprung disease in newbornsAn early symptom in some newborns is failure to have a first bowel movement within 48 hours after birth. Other symptoms may include
Surgery for Hirschsprung diseaseHirschsprung disease is a life-threatening illness, and treatment requires surgery. Children who have surgery for Hirschsprung disease most often feel better after surgery. If growth was slow because of Hirschsprung disease, growth typically improves after surgery.For treatment, a pediatric surgeon will perform a pull-through procedure or an ostomy surgery. During either procedure, the surgeon may remove all or part of the colon, called a colectomy.During a pull-through procedure, a surgeon removes the part of the large intestine that is missing nerve cells and connects the healthy part to the anus. A surgeon most often does a pull-through procedure soon after diagnosis.Ostomy surgery is a surgical procedure that reroutes the normal movement of the stool out of the body when a part of the bowel is removed. Creating an ostomy means bringing part of the intestine through the abdominal wall so that stool can leave the body without passing through the anus. The opening in the abdomen through which stool leaves the body is called a stoma. A removable external collection pouch, called an ostomy pouch or ostomy appliance, is attached to the stoma and worn outside the body to collect the stool. The child or caregiver will need to empty the pouch several times each day.Although most children with Hirschsprung disease do not need ostomy surgery, a child sick from Hirschsprung disease may need ostomy surgery to get better before undergoing the pull-through procedure. This gives the inflamed areas of the intestine time to heal. In most cases, an ostomy is temporary and the child will have a second surgery to close the ostomy and reattach the intestine. However, sometimes children with Hirschsprung disease have a permanent ostomy, especially if a long segment of the bowel is missing nerve cells or the child has repeated episodes of bowel inflammation, which health care providers call enterocolitis.Ostomy surgeries include the following:
How is Hirschsprung disease diagnosed?Making a diagnosis for a genetic or rare disease can often be challenging, and the diagnosis for Hirschsprung disease is based on
How many newborns have Hirschsprung disease?Hirschsprung disease occurs in approximately 1 in 5,000 newborns. Children with Down syndrome and other medical problems, such as congenital heart defects, are at much greater risk. For example, about one in 100 children with Down syndrome also has Hirschsprung disease.Hirschsprung disease is congenital, or present at birth; however, symptoms may or may not be obvious at birth. If you have a child with Hirschsprung disease, your chances of having more children with Hirschsprung disease are greater than people who donât have a child with Hirschsprung disease. Also, if a parent has Hirschsprung disease, the chance of their child having Hirschsprung disease is higher. Talk with your doctor to learn more. What can I expect as my newborn or child recovers from surgery?After surgery, your child will need time to adjust to the new structure of his or her large intestine.Pull-through Procedure RecoveryMost children feel better after the pull-through procedure. However, some children can have complications or problems after surgery. Problems can include
What causes Hirschsprung disease? Is it inherited?Before birth, a child's nerve cells normally grow along the intestines in the direction of the anus. With Hirschsprung disease, the nerve cells stop growing too soon. Why the nerve cells stop growing is unclear. Some Hirschsprung disease is inherited, meaning it is passed from parent to child through genes. Hirschsprung disease is not caused by anything a mother did while pregnant.Isolated Hirschsprung disease can result from mutations in one of several genes, including the RET (most common), EDNRB, and EDN3 genes. However, the genetics of this condition are complex and are not yet completely understood. While a mutation in a single gene sometimes causes the condition, mutations in multiple genes may be required in some cases. The genetic cause of the condition is unknown in approximately half of affected individuals. What is Hirschsprung disease?Hirschsprung disease (HSCR) is a congenital (present at birth) disease of the large intestine or colon. It is one type of birth defect. People with the disease do not have the nerve cells in the intestine required to expel stools from the body normally. |
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