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Secretory meningioma associated with numerous meningothelial rosettes

T Tada1, K Ishii, S Oshima

  • 1Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.

Acta Neuropathologica
|January 1, 1992
PubMed

Insights

This report details a rare secretory meningioma case in a man with moyamoya disease. The tumor displayed numerous meningothelial rosettes, a unique histological finding potentially linked to specific stimuli.

Area of Science:

  • Neuropathology
  • Neurosurgery
  • Oncology

Background:

  • Moyamoya disease is a cerebrovascular disorder characterized by progressive stenosis of intracranial arteries.
  • Meningiomas are tumors arising from the meninges, the membranes surrounding the brain and spinal cord.
  • Secretory meningiomas are a subtype characterized by the presence of psammoma bodies and glandular differentiation.

Observation:

  • A 66-year-old male patient with moyamoya disease presented with progressive skull deformity.
  • Surgical intervention was performed for a skull tumor located over the cerebral hemisphere.
  • Histological examination revealed numerous meningothelial rosettes and pseudopsammoma bodies.

Findings:

  • The case presents a secretory meningioma with an unusually high number of meningothelial rosettes.
  • The observed rosettes bear resemblance to those induced by subarachnoid epinephrine injection and described by Kepes.
  • This represents a potentially novel histological presentation of meningioma.

Implications:

  • This finding expands the histological spectrum of meningiomas, particularly secretory subtypes.
  • Understanding the formation of these rosettes may offer insights into meningioma pathogenesis.
  • Further research is warranted to explore the etiological factors and clinical significance of such rosette formations in meningiomas.

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