- Intestinal atresia
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Intestinal atresia Classification and external resources ICD-10 Q41, Q42 ICD-9 751.1 751.2 OMIM 223400 243600 DiseasesDB 31514 33000 Intestinal atresia is a malformation where there is a narrowing or absence of a portion of the intestine. This defect can either occur in the small or large intestine.
Contents
Types of intestinal atresia
The different types of intestinal atresia are named after their location:
- Duodenal atresia - malformation of the duodenum, part of the intestine that empties from the stomach
- Jejunal atresia - malformation of the jejunum, the second part of the intestine extending from the duodenum to the ileum
- Ileal atresia - malformation of the ileum, the lower part of the small intestine
- Colon atresia - malformation of the colon
Duodenal atresia has a strong association with Down syndrome. It is the most common type, followed by ileal atresia.
Cause
The most common cause of non-duodenal intestinal atresia is a vascular accident in utero that leads to decreased intestinal perfusion and ischemia of the respective segment of bowel. This leads to narrowing, or in the most severe cases, complete obliteration of the intestinal lumen.
In the case that the superior mesenteric artery, or another major intestinal artery, is occluded, large segments of bowel can be entirely underdeveloped. Classically, the affected area of bowel assumes a spiral configuration and is described to have an "apple peel" like appearance; this is accompanied by lack of a dorsal mesentery.
Diagnosis
Intestinal atresias are often discovered before birth: either during a routine sonogram which shows a dilated intestinal segment due to the blockage, or by the development of polyhydramnios (the build up of too much amniotic fluid in the uterus). These abnormalities are indications that the fetus may have a bowel obstruction which a more detailed ultrasound study can confirm.
Some fetuses with bowel obstruction have abnormal chromosomes. An amniocentesis is recommended because it can determine not only the sex of the baby, but whether or not there is a problem with the chromosomes.
Treatment
Fetal and neonatal intestinal atresia are treated using laparotomy after birth. If the area affected is small, the surgeon may be able to remove the damaged portion and join the intestine back together. In instances where the narrowing is longer, or the area is damaged and cannot be used for period of time, a temporary Stoma (medicine) may be placed.
See also
External links
- UCSF Fetal Treatment Center: Bowel Obstructions
- Information about congenital malformations of the gastrointestinal tract in premature babies - The Hospital for Sick Children
Congenital malformations and deformations of digestive system (Q35–Q45, 749–751) Upper GI tract EA/TEF (Esophageal atresia: types A, B, C, and D, Tracheoesophageal fistula: types B, C, D and E)
esophageal rings (Esophageal web · upper, Schatzki ring · lower)Lower GI tract Intestinal atresia (Duodenal atresia) · Meckel's diverticulum · Hirschsprung's disease · Intestinal malrotation · Dolichocolon · Enteric duplication cystAccessory Categories:- Congenital disorders of digestive system
- Disease stubs
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