Abstract

Gliosarcoma (GS) is a malignant neoplasm of the central nervous system that has coexisting glial and mesenchymal components. GSs are rarely related to osseous metaplasia. The authors report a case of GS in a male patient presenting apathy and catatonia. Computed tomography/magnetic resonance imaging showed an expansive process affecting the left frontal lobe. At microscopy, a malignant glioma constituted by highly atypical glial cells intermingled with spindle-shaped cells was identified. The lesion showed areas of necrosis with pseudopalisading formation, focus of osseous metaplasia, and positive immunoexpression of S100, CD99 and vimentin in both elements. Only the sarcomatous component exhibited negative immunoexpression of glial fibrillary acidic protein (GFAP). The diagnosis of GS was then established.

Highlights

  • Gliosarcoma (GS) is considered a glioblastoma variant characterized by the coexistence of glial and mesenchymal components

  • GS is usually located, in decreasing order of frequency, in the temporal (44%), frontal (30%), parietal (28%) and occipital lobes (11%), with rare cases affecting the cerebellum and the spinal cord

  • Unusual cases have been related to systemic metastases

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Summary

Case Report

Metaplasia óssea no gliossarcoma: um achado histológico pouco usual. Gliosarcoma (GS) is a malignant neoplasm of the central nervous system that has coexisting glial and mesenchymal components. GSs are rarely related to osseous metaplasia. The authors report a case of GS in a male patient presenting apathy and catatonia. Computed tomography/magnetic resonance imaging showed an expansive process affecting the left frontal lobe. A malignant glioma constituted by highly atypical glial cells intermingled with spindle-shaped cells was identified. The lesion showed areas of necrosis with pseudopalisading formation, focus of osseous metaplasia, and positive immunoexpression of S100, CD99 and vimentin in both elements. The sarcomatous component exhibited negative immunoexpression of glial fibrillary acidic protein (GFAP).

Case report
Discussion
Findings
Abulia and catatonia Frontal lobe
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