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Primary intracerebral plasma cell granuloma: a light, immunocytochemical, and ultrastructural study of one case

D Figarella-Branger1, D Gambarelli, M Perez-Castillo

  • 1Department of Neuropathology, Centre Hospitalier Regional, Marseille, France.

Neurosurgery
|July 1, 1990
PubMed

Insights

This study presents a rare case of primary intracerebral plasma cell granuloma. The lesion exhibited distinct central fibrous histiocytoma and peripheral plasma cell patterns, with confirmed histiocytic cells.

Area of Science:

  • Neuropathology
  • Oncology
  • Histopathology

Background:

  • Primary intracerebral plasma cell granuloma is an exceptionally rare central nervous system (CNS) tumor.
  • This case presents a unique instance without meningeal involvement, highlighting its distinct characteristics.

Observation:

  • Histological examination revealed a biphasic pattern: a central benign fibrous histiocytoma and a peripheral inflammatory infiltrate.
  • The peripheral infiltrate comprised polyclonal plasma cells, lymphocytes, and cells with epithelial-like morphology.

Findings:

  • Immunocytochemistry and electron microscopy confirmed the histiocytic origin of the 'epithelial-like' cells.
  • The findings suggest a complex histogenesis involving reactive cellular components within the brain parenchyma.

Implications:

  • Understanding the histogenesis and differential diagnosis of such rare CNS lesions is crucial for accurate diagnosis.
  • This case contributes to the limited literature on intracerebral plasma cell granulomas, aiding future research and clinical management.

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