Microscopic anatomy of the brain-meningioma interface.

Brain Tumor Pathol

Department of Neurosurgery, Shiga University of Medical Science, Seta, Ohtsu, Shiga 520-2192, Japan.

Published: August 2009

AI Article Synopsis

  • - The study examined 50 surgical cases of meningiomas and found varying degrees of capsule formation and arachnoid membrane integrity, with correlations to tumor grade and characteristics like size and perifocal edema.
  • - Brain invasion by meningiomas was assessed, revealing GFAP-positive cells in invasive tumors and degenerative changes in surrounding axons, indicating an impact on nearby brain tissue.
  • - The tumors typically showed a collagen type 4-positive boundary, but atypical and anaplastic tumors lacked this feature; no link was found between matrix metalloproteinase expression and arachnoid disruption or brain invasion.

Article Abstract

We analyzed the relation between meningioma and the brain in 50 surgical cases. So-called capsule formation was seen in 20 meningiomas, of which 13 were categorized as thin and 7 as thick. In 21 meningiomas the arachnoid membrane was intact, and 10 meningiomas had no underlying arachnoid membrane. The other 19 tumors showed partial disruption of the arachnoid membrane. The degree of arachnoid disruption correlated with the tumor grade, perifocal edema, pial blood supply on angiography, and tumor size. The existence of brain invasion correlated with the tumor grade and partially with tumor size. In case of invasive tumor, GFAP-positive cells were found deep in the tumor, usually in contact with blood vessels. The axons in gliotic brain often showed degenerative changes such as ballooning or varicose swelling. Meningiomas were usually demarcated by a basement membrane that was collagen type 4 (Col4)-positive. However, atypical and anaplastic meningiomas usually lacked Col4 staining at the interface. In two benign meningiomas that looked like an invasive growth, Col4 staining was seen above the brain. A pia mater-like structure covered the tumor surface in both cases. We could not demonstrate a relation between the expression of matrix metalloproteinase (MMP)-2 or MMP-9 and arachnoid disruption or brain invasion.

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Source
http://dx.doi.org/10.1007/s10014-005-0187-0DOI Listing

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