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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Glioblastoma
equivalentClass
Concept_In_Subset
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Glioblastoma
UMLS_CUI
  • C0017636
Contributing_Source
  • CTEP
ALT_DEFINITION
  • A fast-growing type of central nervous system tumor that forms from glial (supportive) tissue of the brain and spinal cord and has cells that look very different from normal cells. GBM usually occurs in adults and affects the brain more often than the spinal cord.NCI-GLOSS
ICD-O-3_Code
  • 9440/3
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Glioblastoma
FULL_SYN
  • glioblastoma multiformePTNCI-GLOSSCDR0000045699
  • GBMPTNCI-GLOSSCDR0000539131
  • Glioblastoma MultiformeSYNCI
  • GlioblastomaPTNCI
  • Grade IV Astrocytic TumorSYNCI
  • GlioblastomaSYNCITCGA
  • glioblastomaPTNCI-GLOSSCDR0000045698
  • Spongioblastoma MultiformeSYNCI
  • grade IV astrocytomaPTNCI-GLOSSCDR0000044407
  • Glioblastoma multiformePTCTEP10018337
  • Grade IV Astrocytic NeoplasmSYNCI
  • GBM (Glioblastoma)SYNCI
DEFINITION
  • The most malignant astrocytic tumor (WHO grade IV). It is composed of poorly differentiated neoplastic astrocytes and it is characterized by the presence of cellular polymorphism, nuclear atypia, brisk mitotic activity, vascular thrombosis, microvascular proliferation and necrosis. It typically affects adults and is preferentially located in the cerebral hemispheres. It may develop from diffuse astrocytoma WHO grade II or anaplastic astrocytoma (secondary glioblastoma), but more frequently, it manifests after a short clinical history de novo, without evidence of a less malignant precursor lesion (primary glioblastoma). Two histologic variants are recognized: giant cell glioblastoma and gliosarcoma. (WHO)NCI
code
  • C3058
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