Association of small intestinal atresia and Hirschsprung disease in a multi-institutional colorectal registry
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Read the article on pubmed.ncbi.nlm.nih.gov ↗Article · Jun 2026 · 1 min read
In brief
In brief
Multi-institutional registry study identifies rare co-occurrence of jejuno-ileal atresia and Hirschsprung disease in 1% of HSCR patients, with delayed HSCR diagnosis (median 58.5 vs 7 days) and high morbidity including 55.6% developing short bowel syndrome and 100% requiring reoperation within one year.
Written by the GCMD Library team from the article.
Statements in this article
Concomitant jejuno-ileal atresia and Hirschsprung disease occurs in 1.0% of patients with HSCR (15 of 1459 patients in the registry).
Median age at initial surgical consult for patients with both JIA and HSCR was 1 day (IQR 0.5-3.0 days).
Median age at atresia diagnosis in patients with both conditions was 1 day (IQR 0.0-3.0 days).
Median age at HSCR diagnosis in patients with concomitant JIA was 58.5 days (IQR 16-147.5 days), compared to 7 days (IQR 3.0-60.0 days) for patients with HSCR alone.
Ileal atresia was the most common atresia location, occurring in 66.7% of patients (10 of 15).
Total colonic HSCR was present in 60.0% of patients (9 of 15) with concomitant JIA.
HSCR segment length was not consistently related to atresia location.
After primary atresia surgery, 46.7% of patients (7 of 15) had a complication within 30 days.
At one year, 53.3% of patients (8 of 15) required ongoing nutritional support.
At one year, 55.6% of patients (5 of 9) had short bowel syndrome.
At one year, 80.0% of patients (12 of 15) had at least one readmission.
At one year, 100% of patients required at least one reoperation.
Twelve patients (80.0%) have undergone pull-through surgery for HSCR.
