Case report: congenital intraventricular meningioma demonstrated with fetal MRI

Jayant Kumar1, Rahul Lakshmanan2, Jason M Dyke3

  • 1Department of Medical Imaging, Perth Children's Hospital, 15 Hospital Avenue, Nedlands, WA, 6009, Australia. jayantbrij@gmail.com.

Insights

Congenital intraventricular cystic meningioma was identified using fetal MRI, offering early characterization of this rare brain lesion. Fetal MRI is crucial for diagnosing congenital intracranial masses, distinguishing them from other neoplasms.

Area of Science:

  • Neuro-oncology
  • Pediatric Radiology
  • Fetal Medicine

Background:

  • Congenital intracranial meningiomas are exceptionally rare tumors.
  • Intraventricular meningiomas are more frequently observed in pediatric populations compared to adults.

Observation:

  • A case of congenital intraventricular cystic meningioma was identified and characterized using fetal magnetic resonance imaging (MRI).
  • This represents the first in vivo description of a congenital meningioma visualized with fetal MRI.
  • Fetal MRI successfully differentiated the intraventricular mass from choroid plexus neoplasms by demonstrating its separation from the choroid plexus.

Findings:

  • The fetal MRI provided detailed characterization of the atypical intraventricular mass.
  • Histopathology confirmed the diagnosis postnatally.
  • The lesion's intraventricular location was noted, aligning with pediatric prevalence.

Implications:

  • Meningioma should be included in the differential diagnosis for congenital intraventricular lesions detected prenatally.
  • Fetal MRI is a valuable tool for the in vivo characterization and diagnosis of congenital intracranial masses.
  • Early and accurate diagnosis via fetal MRI can guide appropriate management strategies for affected infants.

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