The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 251630
A rare glial tumor characterized by a grade III oligodendroglial tumour with focal or diffuse anaplastic features. It typically occurs in the supratentorial white matter. Histologically, the cells are enlarged and epithelioid with pleomorphic and increased size nuclei, a vesicular chromatin pattern and prominent nucleoli. Most patients present with seizures.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
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