loading...| Preferred Name | Anaplastic oligodendroglioma | |
| Synonyms |
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| Definitions |
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. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_251630 |
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| definition |
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. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=251630 |
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| has_age_of_onset |
Adult |
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| has_inheritance |
Not applicable |
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| hasDbXref |
ICD-11:XH8844 ICD-11:2A00.0Y OMIM:137800 ICD-11:XH9QF3 ICD-10:C71.9 UMLS:C0334590 MedDRA:10026659 |
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| label |
Anaplastic oligodendroglioma |
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| notation |
ORPHA:251630 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_251630 |
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| prefLabel |
Anaplastic oligodendroglioma |
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| present_in |
Europe AND has_annual_incidence_average_value : 0.09 AND has_annual_incidence_range : <1 / 1 000 000 United States AND has_annual_incidence_average_value : 0.11 AND has_annual_incidence_range : 1-9 / 1 000 000 |
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| treeView | ||
| subClassOf |