[A clear cell type meningioma in the upper eyelid ascertained by immunohistochemical examination]

S Harada1, D Watanabe, H Kaneko

  • 1Department of Ophthalmology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

Insights

This report details a rare clear cell meningioma in the upper eyelid. Immunohistochemistry confirmed the diagnosis, highlighting its value in identifying uncommon meningioma subtypes.

Area of Science:

  • Ophthalmology
  • Neuropathology
  • Oncology

Background:

  • Meningiomas are rare tumors originating from meninges.
  • Clear cell meningioma is an uncommon subtype with distinct histological features.
  • Eyelid involvement by meningioma is exceptionally rare.

Observation:

  • A 66-year-old male presented with a slow-growing, well-defined tumor in the left upper eyelid.
  • Computed tomography revealed a homogeneous, contrast-enhancing mass.
  • Histological examination showed oval cells with clear cytoplasm in streamed and whorl patterns, lacking psammoma bodies or calcification.

Findings:

  • Immunohistochemistry revealed positivity for vimentin, epithelial membrane antigen, and protein S-100.
  • These markers are characteristic of meningioma cells.
  • The histological and immunohistochemical profile confirmed a clear cell meningioma.

Implications:

  • Eyelid meningiomas may arise from ectopic arachnoid cells associated with the trigeminal nerve sheath.
  • Histological and immunohistochemical variability necessitates careful diagnostic evaluation.
  • Accurate diagnosis is crucial for appropriate management and understanding of rare orbital tumors.
Abstract

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