Primary extracranial meningioma of the sinonasal tract

M Petrulionis1, N Valeviciene, I Paulauskiene

  • 1Clinic of Ear, Nose and Throat Disease and Clinic of Pulmonology and Radiology, Vilnius University Hospital Santariskiu Klinikos, Vilnius, Lithuania.

Insights

This study details an extracranial meningioma in an 8-year-old child, successfully treated with surgery. The rare sinonasal tract tumor showed no recurrence after 6 months.

Area of Science:

  • Neuro-oncology
  • Pediatric Neurosurgery

Background:

  • Meningiomas typically arise within the central nervous system.
  • Extracranial meningiomas are rare, with sinonasal tract involvement being particularly uncommon.
  • Primary extracranial meningiomas can occur in the nasal cavity, paranasal sinuses, and nasopharynx.

Observation:

  • An 8-year-old child presented with left nostril obstruction and left eye tearing.
  • Magnetic resonance imaging (MRI) revealed a tumor in the left lower, middle turbinate, and ethmoidal cells.
  • Computed tomography (CT) and histological evaluation were performed alongside MRI.

Findings:

  • The tumor was surgically removed (extirpated).
  • Histological examination identified the tumor as a meningothelial meningioma.
  • The diagnosis was confirmed as an extracranial meningioma of the sinonasal tract based on clinical, radiological, and histological data.

Implications:

  • This case highlights the possibility of primary meningiomas in the sinonasal region.
  • Successful surgical management of sinonasal meningiomas is demonstrated.
  • The findings support the importance of comprehensive evaluation for rare pediatric sinonasal tumors.