Abstract
Intestinal neuronal dysplasia is one of the most commonly encountered variant of Hirschsprung’s disease but also in that untreated cases may prove fatal. The authors describe the operative treatment for a newborn who was diagnosed with long segmental intestinal neuronal dysplasia, as the remains of the normal bowel was no more than 35 centimeters from the DJ junction. The side-to-side enteroenterostomy of the affected intestine with Santulli enterostomy could rescue the baby from parenteral nutrition, regaining normal oral feeding.
| Original language | English |
|---|---|
| Pages (from-to) | S209-S213 |
| Journal | Journal of the Medical Association of Thailand |
| Volume | 100 |
| Issue number | 5 |
| Publication status | Published - May 2017 |
Keywords
- IND
- Intestinal neuronal dysplasia
- NID
- Neuronal intestinal dysplasia
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