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Bowel Atresia

Definition

Group of conditions where segment of bowel fails to develop a lumen (patent hole) and is therefore blocked.

Can occur at any point along bowel length

  • Oesophageal (throat)
  • Duodenal
  • Jejeno-ileal (small bowel)
  • Large bowel
  • Anal
Incidence 1:1000 live births
Diagnosis Ultrasound features dependent on level of blockage.  For example oesophageal associated with polyhydramnios (due to problems swallowing amniotic fluid), whereas anal associated with large bowel dilatation
Gestation at diagnosis Depends on level of blockage.  Commonly 20 weeks onwards, but may be later or even after birth (50% of anal atresia diagnosed postnatally)
Known cause, chromosomal or genetic association Upper blockage levels are associated with chromosomal abnormalities (5% of oesophageal and duodenal). Lowe levels (jejunal, ileal) not associated with chromosomal or genetic problems in isolation. Anal atresia is associated with alcohol, diabetes and VACTERL
Further investigations Karyotype if upper bowel levels
Differential Diaganosis Other abdominal abnormalities that can give rise to similar appearances e.g. diaphragmatic hernia, duplication cysts, ovarian cysts etc.
Prognosis If isolated usually good though all will require neonatal surgery and may result in a prolonged hospital stay due to feeding difficulties. If large segments of bowel missing may have significant problems with weight gain.
Recurrance risk Low
Research Studies  

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