Nasal glial heterotopia in children: Two case reports and literature review

Int J Pediatr Otorhinolaryngol. 2020 Feb:129:109728. doi: 10.1016/j.ijporl.2019.109728. Epub 2019 Oct 15.

Abstract

Nasal glial heterotopia is a rare developmental anomaly. We present two cases of nasal glial heterotopia. The presenting symptoms, imaging findings, treatment, histological appearance, and follow-up are described in detail. We additionally reviewed all pediatric cases of nasal glial heterotopia published between 1980 and 2018 in the PubMed and Baidu Scholar databases. We identified 60 pediatric patients (36 [60%] boys). The main symptoms were nasal congestion and open-mouth breathing. Treatment was successful in all patients, and the recurrence rate was low (3/60, 5%). Nasal glial heterotopia requires multidisciplinary management but has a good prognosis.

Keywords: Children; Congenital nasal lesion; Encephalocele; Glial heterotopia; Nasal.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child, Preschool
  • Choristoma / complications
  • Choristoma / diagnosis*
  • Choristoma / surgery*
  • Female
  • Humans
  • Infant
  • Mouth Breathing / etiology
  • Nasal Obstruction / etiology
  • Neuroglia*
  • Nose Diseases / complications
  • Nose Diseases / diagnosis*
  • Nose Diseases / surgery*