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Tricks - Ultrashort Segment Hirschsprungs - Kristine Thayer

Video Published 2018-11-10 Updated 2026-06-02

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Topic Overview

Case discussion of a 16-year-old with Down syndrome presenting with lifelong constipation, diagnosed with ultrashort segment Hirschsprung disease via transanal rectal biopsy showing absent ganglion cells and abnormal calretinin staining. Faculty debate optimal surgical approach (Duhamel vs. transanal pull-through) and whether diverting stoma is needed given patient's age and relatively non-dilated colon.

Key Takeaways

  • Suction rectal biopsy in older patients requires adequate submucosa, correct anatomic level, nerve hypertrophy assessment, and calretinin staining.
  • Ultra-short segment Hirschsprung's in adolescents may present with chronic constipation without enterocolitis or classic transition zone on imaging.
  • In older patients with dilated colon, consider staged approach with diverting stoma before definitive pull-through to allow colonic decompression.
  • Duhamel procedure may be preferable to transanal pull-through in adolescents to avoid excessive sphincter stretching with thick rectal wall.
  • Functional outcomes should guide surgical decision-making in ultra-short segment disease—pathologic findings alone may not justify intervention.

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