About: Synovial Sarcoma     Goto   Sponge   NotDistinct   Permalink

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

AttributesValues
rdf:type
rdfs:label
  • Synovial Sarcoma
equivalentClass
Concept_In_Subset
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Synovial Sarcoma
UMLS_CUI
  • C0039101
Contributing_Source
  • CDISC
  • CTEP
ALT_DEFINITION
  • A malignant tumor that develops in the synovial membrane of the joints.NCI-GLOSS
  • A malignant neoplasm that usually arises in the synovial membranes of the joints and the synovial cells of the tendons and bursae.CDISC
ICD-O-3_Code
  • 9040/3
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Synovial_Sarcoma
FULL_SYN
  • SSABNCI
  • SSSYCDISC
  • Synovial SarcomaPTNCI
  • Synovial sarcomaPTCTEP10042866
  • SARCOMA, SYNOVIAL, MALIGNANTPTCDISC
  • synovial sarcomaPTNCI-GLOSSCDR0000044626
DEFINITION
  • A malignant neoplasm characterized by the chromosomal translocation t(X;18)(p11;q11). It can occur at any age, but mainly affects young adults, more commonly males. Although any site can be affected, the vast majority of the cases arise in the deep soft tissues of extremities, especially around the knee. Microscopically, synovial sarcoma is classified as monophasic (with a spindle or epithelial cell component) or biphasic (with both spindle and epithelial cell components). Synovial sarcomas can recur or metastasize to the lungs, bones, and lymph nodes.NCI
code
  • C3400
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