Journal of Clinical and Diagnostic Research (Oct 2015)

Intraparenchymal Angiomatous Meningioma: A Diagnostic Dilemma

  • DIVYA BANSAL,
  • PREETI DIWAKER,
  • PRIYANKA GOGOI,
  • WAZID NAZIR,
  • ANUPAMA TANDON

DOI
https://doi.org/10.7860/JCDR/2015/15950.6602
Journal volume & issue
Vol. 9, no. 10
pp. ED07 – ED08

Abstract

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Meningioma arises from the arachnoid cap cells of the cerebrum. Intraparenchymal meningiomas or meningiomas without dural attachment are rare. We report a case of 40-year-old male who presented with a history of headache, dizziness and gradual loss of vision since one year. Clinicoradiological diagnosis of a high grade glioma was considered. Tumour was excised and haematoxylin and eosin stained sections revealed a tumour comprised predominantly of variable sized blood vessels showing hyalinization in a background of plump spindle cells with oval vesicular nuclei. In view of these features angiomatous meningioma was suspected. However, to confirm the diagnosis, a panel of immunohistochemical markers including vimentin, EMA and GFAP was done and a final diagnosis of angiomatous meningioma was offered. Angiomatous meningioma is a rare variant of meningioma and even much rarer in the intraparenchymal location. Angiomatous meningioma should be considered in the differential diagnosis of highly vascular intraparenchymal brain tumours.

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