About: Synovial Sarcoma

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Attributes	Values
rdf:type	Class
rdfs:label	Synovial Sarcoma
equivalentClass	nodeID://b640208
Concept_In_Subset	NCI CTEP Simplified Disease Classification Terminology NCI CTEP SDC Non-Rhabdomyosarcoma Soft Tissue Sarcoma Sub-Category Terminology Clinical Data Interchange Standards Consortium Terminology CDISC SDTM Terminology CDISC SEND Terminology CDISC SEND Tumor Findings Results Terminology
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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