Locations Main Campus: Chesterfield, MO 63017   |   Locations
314-434-1500 314-434-1500   |   Contact Us

Multimedia Encyclopedia


 
E-mail Form
Email Results

 
 
Print-Friendly
Bookmarks
bookmarks-menu

Omphalocele

Birth defect - omphalocele; Abdominal wall defect - infant; Abdominal wall defect - neonate; Abdominal wall defect - newborn

 

An omphalocele is a birth defect in which an infant's intestine or other abdominal organs are outside of the body because of a hole in the belly button (navel) area. The intestines are covered only by a thin layer of tissue and can be easily seen.

Causes

 

Omphalocele is considered an abdominal wall defect (a hole in the abdominal wall). The child's intestines usually stick out (protrude) through the hole.

The condition looks similar to gastroschisis. An omphalocele is a birth defect in which the infant's intestine or other abdominal organs protrude through a hole in the belly button area and are covered with a membrane. In gastroschisis, there is no covering membrane.

Abdominal wall defects develop as a baby grows inside the mother's womb. During development, the intestine and other organs (liver, bladder, stomach, and ovary or testes) develop outside the body at first and then usually return inside. In babies with omphalocele, the intestine and other organs remain outside the abdominal wall, with a membrane covering them. The exact cause for abdominal wall defects is not known.

Infants with an omphalocele often have other birth defects. Defects include genetic problems (chromosomal abnormalities), congenital diaphragmatic hernia, and heart and kidney defects.

 

Symptoms

 

An omphalocele can be clearly seen. This is because the abdominal contents stick out (protrude) through the belly button area.

There are different sizes of omphaloceles. In small ones, only the intestines remain outside the body. In larger ones, the liver or other organs may be outside as well.

 

Exams and Tests

 

Prenatal ultrasounds often identify infants with an omphalocele before birth.

Testing is often not necessary to diagnose omphalocele. But, babies with an omphalocele should be tested for other problems that often go with it. This includes ultrasounds of kidneys and heart, blood tests for genetic disorders, among other tests.

 

Treatment

 

Omphaloceles are repaired with surgery , although not always immediately. A sac protects the abdominal contents and may allow time for other more serious problems (such as heart defects) to be dealt with first, if necessary.

To fix an omphalocele, the sac is covered with a special man-made material, which is then stitched in place to form what is called a silo. As the baby grows over time, the abdominal contents are pushed into the abdomen.

When the omphalocele can comfortably fit within the abdominal cavity, the silo is removed and the abdomen is closed.

Sometimes, the omphalocele is so large that it cannot be placed back inside the infant's abdomen. The skin around the omphalocele grows and eventually covers the omphalocele. The abdominal muscles and skin can be repaired when the child is older for a better cosmetic outcome.

 

Outlook (Prognosis)

 

Complete recovery is expected after surgery for an omphalocele. However, omphaloceles often occur with other birth defects. How well a child does depends on which other conditions the child has.

If the omphalocele is identified before birth, the mother should be closely monitored to make sure the unborn baby remains healthy.

Plans should be made for careful delivery and immediate management of the problem after birth. The baby should be delivered in a medical center that is skilled at repairing abdominal wall defects. The baby is likely to do better if they do not need to be taken to another center for further treatment.

Parents should consider testing the baby and possibly family members for other genetic problems that are associated with this condition.

 

Possible Complications

 

The misplaced abdominal contents can make it difficult for the baby to expand the lungs, leading to breathing problems.

Another complication is bowel death. This occurs when intestinal tissue dies due to low blood flow or infection.

This condition is apparent at birth and will be detected in the hospital at delivery if it has not already been seen on routine fetal ultrasound exams during pregnancy. If you have given birth at home and your baby appears to have this defect, call the local emergency number (such as 911) right away.

 

When to Contact a Medical Professional

 

This problem is diagnosed and repaired in the hospital at birth. After returning home, call your health care provider if your baby develops any of these symptoms:

  • Decreased bowel movements
  • Feeding problems
  • Fever
  • Green or yellowish green vomit
  • Swollen belly area
  • Vomiting (different than normal baby spit-up)
  • Worrisome behavioral changes

 

 

References

Islam S. Congenital abdominal wall defects. In: Holcomb GW, Murphy JP, Ostlie DJ, eds. Ashcraft's Pediatric Surgery . 6th ed. Philadelphia, PA: Elsevier Saunders; 2014:chap 48.

Walther AE, Nathan JD. Newborn abdominal wall defects. In: Wylie R, Hyams JS, Kay M, eds. Pediatric Gastrointestinal and Liver Disease . 5th ed. Philadelphia, PA: Elsevier; 2016:chap 58.

 
  • Infant omphalocele - illustration

    An omphalocele is an abdominal wall defect at the base of the umbilical cord (umbilicus); the infant is born with sac protruding through the defect which contains small intestine, liver, and large intestine.

    Infant omphalocele

    illustration

  • Omphalocele repair - series

    Presentation

  •  
    • Infant omphalocele - illustration

      An omphalocele is an abdominal wall defect at the base of the umbilical cord (umbilicus); the infant is born with sac protruding through the defect which contains small intestine, liver, and large intestine.

      Infant omphalocele

      illustration

    • Omphalocele repair - series

      Presentation

    •  

     

    Review Date: 11/3/2015

    Reviewed By: Kimberly G Lee, MD, MSc, IBCLC, Associate Professor of Pediatrics, Division of Neonatology, Medical University of South Carolina, Charleston, SC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.

    The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997- A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

     
     
     

     

     

    A.D.A.M. content is best viewed in IE9 or above, Firefox and Google Chrome browser.



    Content is best viewed in IE9 or above, Firefox and Google Chrome browser.