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Meningiomas in children: MR and histopathologic findings

C M Glasier1, M M Husain, W Chadduck

  • 1Department of Radiology, Arkansas Children's Hospital, Little Rock 72202.

Abstract

Insights

Pediatric meningiomas, often extra-axial, present differently than adult tumors. Magnetic resonance (MR) imaging and histopathology reveal key diagnostic features in children with these brain tumors.

Area of Science:

  • Pediatric neuro-oncology
  • Neuroradiology
  • Molecular genetics

Background:

  • Meningiomas are uncommon in children but represent a significant portion of primary pediatric brain tumors.
  • Understanding the unique characteristics of pediatric meningiomas is crucial for diagnosis and treatment planning.

Purpose of the Study:

  • To detail the magnetic resonance (MR) imaging and histopathologic findings in a cohort of five pediatric patients diagnosed with meningiomas.
  • To compare the findings in children with those typically observed in adult meningiomas.

Main Methods:

  • Retrospective analysis of preoperative contrast-enhanced MR imaging in five children (3 months to 16 years) with pathologically confirmed meningiomas.
  • Histopathologic examination of tumor tissue, including chromosomal analysis for chromosome 22 abnormalities in four patients.

Main Results:

  • All five meningiomas were extra-axial, with two supratentorial and three in the posterior fossa.
  • MR imaging demonstrated variable precontrast T1 signal, hyperintensity on proton density and T2-weighted images, and intense postcontrast enhancement.
  • Histopathology revealed diverse subtypes, including meningotheliomatous, transitional, chordoid, and hemangiopericytic variants. Two of four tumors showed chromosome 22 deletions.

Conclusions:

  • Pediatric meningiomas exhibit a predilection for posterior fossa location and a broader range of histologic subtypes compared to adult meningiomas.
  • Characteristic MR imaging features include extra-axial location, specific signal intensities, and strong contrast enhancement.
  • Chromosomal aberrations, particularly involving chromosome 22, are observed in a subset of pediatric meningiomas.

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