Lymphoplasmacyte-rich meningioma: a case report with histological and immunohistochemical studies

M Mizushima1, Y Tanaka, S Kawakami

  • 1Division of Neurosurgery, Faculty of Medicine, Tottori University, Yonago, Japan.

Brain Tumor Pathology
|January 1, 1997
PubMed

Insights

A rare lymphoplasmacyte-rich meningioma in a 64-year-old woman mimicked ordinary meningioma. Immunohistochemistry revealed the lymphocytic infiltrate was likely a host immune response, not a neoplastic process.

Area of Science:

  • Neuropathology
  • Immunohistochemistry
  • Neoplastic Pathology

Background:

  • Meningiomas are common primary brain tumors, typically benign and slow-growing.
  • Lymphoplasmacyte-rich meningiomas represent a rare variant with distinct histological features.
  • Distinguishing neoplastic from reactive cellular components is crucial for accurate diagnosis.

Observation:

  • A 64-year-old female patient presented with a tumor exhibiting typical meningioma radiographic and macroscopic appearance.
  • Immunohistochemical staining of meningothelial cell components was positive for epithelial membrane antigen.
  • Analysis of lymphocyte surface markers (L26, UCHL-1) was performed on the tumor infiltrate.

Findings:

  • The meningothelial cells confirmed the diagnosis of meningioma.
  • The lymphoplasmacytic proliferation within the tumor was negative for neoplastic markers.
  • Immunohistochemical results strongly suggested the infiltrate represented a host immune response rather than a neoplastic proliferation.

Implications:

  • This case highlights the importance of comprehensive immunohistochemical analysis in diagnosing rare meningioma variants.
  • Understanding the nature of the lymphoplasmacytic infiltrate can refine diagnostic criteria for lymphoplasmacyte-rich meningiomas.
  • Differentiating reactive immune cells from neoplastic lymphocytes is critical for appropriate patient management and prognosis.

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