About: Extraskeletal Myxoid Chondrosarcoma     Goto   Sponge   NotDistinct   Permalink

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

AttributesValues
rdf:type
rdfs:label
  • Extraskeletal Myxoid Chondrosarcoma
equivalentClass
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Extraskeletal Myxoid Chondrosarcoma
UMLS_CUI
  • C1275278
ALT_DEFINITION
  • A malignant soft tissue tumor characterized by multinodular architecture, abundant myxoid matrix and malignant chondroblast-like cells arranged in cords, clusters or delicate networks. There are recurrent cytogenetic aberrations: t(9;22)(q22;q12) and t(9;17)(q22;q11).NCI
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Myxoid_Extraskeletal_Chondrosarcoma
FULL_SYN
  • Extraosseous ChondrosarcomaSYNCI
  • Myxoid Extraosseous ChondrosarcomaSYNCI
  • Myxoid Extraskeletal ChondrosarcomaSYNCI
  • Extraskeletal Myxoid ChondrosarcomaPTNCI
  • EMCABNCI
  • Extraskeletal ChondrosarcomaSYNCI
DEFINITION
  • A rare malignant soft tissue neoplasm of uncertain lineage characterized by the presence of chondroblast-like cells in a myxoid stroma and a multinodular growth pattern. The most common sites of involvement are the deep soft tissues of the extremities, particularly the thigh. It usually presents as an enlarging soft tissue mass. Patients may have long survivals, but local recurrences and metastases occur in approximately half of the cases. The most common site of metastasis is the lungs.NCI
code
  • C27502
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