COMPOSITE PLEOMORPHIC XANTHOASTROCYTOMA-GANGLIOGLIOMA; ASSESSING AND ADDRESSING THE DILEMMA OF DIFFERENTIAL EXPRESSION OF NEURONAL MARKERS: CASE REPORT WITH DIAGNOSTIC PERSPECTIVE

Composite pleomorphic xanthoastrocytoma-ganglioglioma; assessing and addressing the dilemma of differential expression of neuronal markers: Case report with diagnostic perspective

Composite pleomorphic xanthoastrocytoma-ganglioglioma; assessing and addressing the dilemma of differential expression of neuronal markers: Case report with diagnostic perspective

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We report the case of a 5-year-old male child presenting with seizures for 4 months.Magnetic resonance imaging (MRI) revealed a cortical-based solid cystic lesion in the right parietal lobe.Histopathological examination showed a tumour comprised of spindled glial fibrillary acid protein (GFAP) positive neoplastic cells interspersed with bizarre pleomorphic RXOMEGA-3 600MG cells showing nuclear pseudoinclusions and intermingled dysplastic ganglion cells variably immunopositive for synaptophysin, chromogranin, Neu-N and immunonegative hardware for neuron filament protein (NFP).This report highlights the occurrence of the rare composite pleomorphic xanthoastrocytoma-ganglioglioma and the vagaries of immunohistochemical analysis in highlighting neuronal differentiation in such a case setting.In addition, to the best of our knowledge this is the youngest patient till date to present with this entity.

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