Histiocytic meningioma: A distinctive subtype of meningioma?

Liqiong Liu1, Jonathan Stone2, Joan T Hoffpauir3

  • 1Louisiana State University Health Science Center, New Orleans, USA;

Insights

This study details a rare case of histiocytic meningioma in a 55-year-old woman, characterized by significant histiocytic infiltration. Researchers propose classifying this distinct meningioma subtype based on its unique pathological features.

Area of Science:

  • Neuropathology
  • Oncology
  • Histopathology

Background:

  • Meningiomas are typically slow-growing tumors arising from the meninges.
  • Histiocytic changes within meningiomas are exceptionally uncommon, presenting diagnostic challenges.

Observation:

  • A 55-year-old female presented with a four-year history of progressive headache and cognitive decline.
  • MRI revealed a well-defined, contrast-enhancing lesion in the right superior frontoparietal region.
  • Histopathological analysis showed a meningioma with approximately 50% histiocytic infiltration.

Findings:

  • Immunohistochemistry confirmed neoplastic meningothelial cells and histiocytic cells expressing epithelial membrane antigen (EMA).
  • Histiocytic cells were positive for CD4 and CD68, with scattered S100-positive cells.
  • The Ki67 proliferation index was low (1.6%), with no signs of high-grade malignancy or invasion.

Implications:

  • The findings suggest that histiocytic meningioma may represent a distinct subtype requiring specific diagnostic criteria.
  • Further research into the biological basis and differential diagnosis of this rare entity is warranted.
  • Accurate classification is crucial for appropriate patient management and prognosis.

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