|
|
|
|
|
|
| Abdominal Wall Defects (Congenital) |
| Etiology Abdominal wall defects include omphalocele, gastroschisis, limb-body wall complex and prune-belly syndrome. Although grouped together, their etiology and pathogenesis may vary. Omphalocele is associated with other anomalies (50%); many have trisomy 18; neural-tube defects are also common. Gastroschisis and limb body wall complex is not associated with other anomalies or chromosome abnormalities. Prune-Belly syndrome is associated with intestinal abnormalities. |
| Pathogenesis Omphalocele is a defect at the umbilicus. Gastroschisis is a defect lateral to the midline; theories include either ischemia (interruption of the omphalomesenteric artery). Limb-body wall complex (body stalk anomaly) is a major disruption which may be due to rupture of the amniotic sac with adhesion to the placenta. Ischemia is also invoked. Prune-belly is theorized to result either from a defect in the "mesoderm" or secondary to abdominal distention., |
| Epidemiology Omphalocele most common; prune belly most abnormal. Male=female Associated with fetal loss. |
| General Gross Description The intestine and other portions of the abdominal organs herniate omphalocele, limb-body wall complex and gastroschisis. The major differentiation is the location of the defect (umbilical or lateral to the midline) and the associated anomalies. |
| General Microscopic Description Little microscopic abnormality. |
| Clinical Correlation Although frequently fatal in utero, gastroschisis and omphalocele can be repaired. Morbidity and mortality revolve around associated abnormalities in the bowel and other organs. |
| References Developmental Pathology of the Embryo and Fetus. Dimmick JE, Kalousek DK (eds). Philadelphia: Lippincott, 1992, pp. 527-9. |
| Abdominal Wall Defects (Congenital) |
| Synopsis by: Melinda Sanders M.D. (T89000M28100)[613] |
| Search Medline at National Library of Medicine Please be patient during transfer. Medline will open in a new window. To return, close the Medline Window |
|
|
|
|
|
|