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Intestinal ganglioneuromatosis of the ileum and colon in a pediatric patient: a case report associated with Noonan syndrome

  • Carvajalino Galeano Ana Beatriz
  • , Garcia Garzon Gabriela
  • , Ebratt Rincon Angie
  • , Vargas Magda Jimena
  • , Mercedes Olaya-C

Research output: Contribution to journalArticlepeer-review

Abstract

Intestinal ganglioneuromatosis (GNM) is a rare condition classified among gastrointestinal motility disorders, which are commonly associated with chronic constipation. This entity predominantly affects pediatric patients, often in the context of systemic syndromes. We report the case of a 6-year-old male who presented with abdominal pain, vomiting, and constipation. Following surgical intervention, histopathological examination of the resected intestinal segment confirmed the diagnosis of GNM. Subsequent genetic evaluation revealed phenotypic features consistent with Noonan syndrome. In pediatric patients, constipation remains one of the most challenging disorders to manage. In cases of GNM, it is essential to assess potential associations with genetic syndromes, given their known predisposition to tumorigenesis. To the best of our knowledge, this is the first reported case describing an association between Noonan syndrome and intestinal ganglioneuromatosis.

Original languageEnglish
Article number300788
Pages (from-to)1-4
Number of pages4
JournalHuman Pathology Reports
Volume41
DOIs
StatePublished - Sep 2025

Keywords

  • Enteric nervous system
  • Enteric plexus hyperplasia
  • Intestinal ganglioneuromatosis
  • Intestinal obstruction
  • Noonan syndrome

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