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[Meningioma of the lateral ventricle. 3 recent cases]

P Bret1, S Gharbi, F Cohadon

  • 1Service de Neurochirurgie C, U.F.R. Lyon Nord et Alexis-Carrel, Hôpital Neurologique et Neurochirurgical Pierre-Wertheimer.

Neuro-Chirurgie
|January 1, 1989
PubMed

Insights

Intraventricular meningiomas are rare intracranial tumors. Diagnosis is typically made with CT scans, though MRI can be helpful, and surgical removal is often straightforward.

Area of Science:

  • Neurosurgery
  • Neuropathology
  • Neuroradiology

Background:

  • Intraventricular meningiomas are rare, comprising only 0.2% of intracranial neoplasms and 2% of adult meningiomas.
  • These tumors arise from meningothelial inclusions within the arachnoid of the tela choroidea.

Observation:

  • Three cases are presented: two in the right trigonal area and one in the left occipital horn of a 14-year-old girl.
  • Clinical presentation can include paroxysmal increased intracranial pressure, potentially due to intraventricular bleeding rather than a trapped ventricular horn.

Findings:

  • CT scans typically reveal a hyperdense, enhancing mass attached to the choroid plexus.
  • MRI findings can vary, with one case showing low T1 and high T2 signal intensity; another case presented as a cystic lesion on MRI.
  • Angiography is useful for identifying the primary blood supply, mainly from the posterolateral choroidal arteries.

Implications:

  • Despite their rarity, intraventricular meningiomas are usually diagnosed preoperatively using imaging techniques.
  • Surgical approaches, such as the transfrontal approach for tumors near the foramen of Monro, are often technically manageable.

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