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Jejunoileal atresia and associated malformations: correlation with the timing of in utero insult
1Children's Research Centre, Our Lady's Hospital for Sick Children, Dublin, Ireland.
Insights
Jejunal atresia (JA) is linked to more major congenital malformations than ileal atresia (IA). This suggests some jejunal atresias may stem from a developmental issue, unlike ileal atresias.
Area of Science:
- Pediatric Surgery
- Congenital Malformations
- Gastrointestinal Development
Background:
- Duodenal atresia is associated with more congenital anomalies than jejunoileal atresia.
- This observation supports early fetal obstruction as the cause of duodenal atresia.
Purpose of the Study:
- To investigate the correlation between the location of jejunoileal atresia and associated major congenital malformations.
- To determine if jejunal atresia (JA) has a higher incidence of anomalies compared to ileal atresia (IA).
Main Methods:
- Retrospective review of jejunoileal atresia cases treated between 1980 and 1997.
- Analysis of patient records to identify associated major congenital malformations.
Main Results:
- Of 83 patients, 38 had JA and 45 had IA.
- Associated major malformations were found in 42% of JA patients versus 2% of IA patients.
- Multiple or apple-peel atresias were present in 53% of JA patients, compared to single atresias in 91% of IA patients.
Conclusions:
- Jejunal atresia exhibits a significantly higher incidence of associated major extraintestinal congenital malformations than ileal atresia.
- These findings suggest a potential malformative etiology for some cases of jejunal atresia.
Purpose:
Duodenal atresia is associated with a higher incidence of associated congenital malformations than jejunoileal atresia, supporting the hypothesis that the duodenal obstruction occurs early in fetal life. In this study, the authors analyzed the incidence of major associated malformations in jejunal atresia (JA) and ileal atresia (IA) to determine if there is a positive correlation between the proximity of the intestinal atresia and the association of other major anomalies.
Methods:
Records of all patients with jejunoileal atresias treated at the authors' institution between 1980 and 1997 were examined.
Results:
There were 83 patients with jejunoileal atresias, 38 with JA, and 45 with IA. Sixteen (42%) of the JA patients had an associated major congenital malformation, whereas only 1 (2%) of the IA patients had an associated malformation. A single atresia was found in 18 (47%) of JA patients and 41 (91%) of IA patients. Twenty (53%) of the JA patients had either multiple or apple-peel atresia. Thirteen patients (16%) died, 11 with JA, and 2 with IA. Of the 11 patients with JA who died, 6 had multiple atresias, 4 had cystic fibrosis, and 1 had small bowel volvulus.
Conclusion:
The higher incidence of associated major congenital extraintestinal malformations in JA compared with IA patients suggests that some cases of JA may arise from a malformative process.
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