Recurrent Childhood Pleomorphic Xanthoastrocytoma

Preferred Label : Recurrent Childhood Pleomorphic Xanthoastrocytoma;

NCIt related terms : Recurrent Pleomorphic Xanthoastrocytoma;

NCIt definition : The reemergence of pleomorphic xanthoastrocytoma in childhood after a period of remission.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL433943;

Details

Origin ID

C115375;

UMLS CUI

C3897744;

Disease may have findings
- Eosinophilic Granular Bodies Present [NCIt concept]
- Favorable Clinical Outcome [NCIt concept]
- Seizure [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_finding
- Anaplastic Lesion [NCIt concept]
- Grade 4 Lesion [NCIt concept]
- Precise Histogenesis Unknown [NCIt concept]
disease_has_abnormal_cell
- Giant Astrocyte [NCIt concept]
- Neoplastic Astrocyte [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Glial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell and Neoplastic Perineural Cell [NCIt concept]
- Xanthomatous Astrocyte [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Dense Intercellular Reticulin Network Present [NCIt concept]
- Intracellular Accumulation of Lipids [NCIt concept]
- Lymphocytic Infiltrate [NCIt concept]
- Recurrent Disease [NCIt concept]
disease_has_grade
- Grade 2 [NCIt concept]
- Low Grade [NCIt concept]
disease_has_normal_cell_origin
- Astrocyte [NCIt concept]
- Glial Cell [NCIt concept]
- Neuroepithelial Cell [NCIt concept]
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
disease_has_normal_tissue_origin
- Nerve Tissue, Neuroepithelial Tissue, and Nerve Sheaths [NCIt concept]
- Neuroepithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 3 [NCIt concept]
- Gain of Chromosome 7 [NCIt concept]
disease_may_have_molecular_abnormality
- BRAF NP_004324.2:p.V600E [NCIt concept]
- Homozygous CDKN2A Gene Deletion [NCIt concept]
- Homozygous CDKN2B Gene Deletion [NCIt concept]

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