ossifying fibromyxoid tumor
A rare soft tissue tumor of uncertain lineage characterized by the presence of neoplastic spindle to round cells forming cords in a fibromyxoid stroma. The lesions are associated with the formation of metaplastic bone. Most patients present with painless subcutaneous masses. Recurrences have been reported in a minority of patients. [ NCIT:P378 ]
Term info
- SCTID:404076001 (MONDO:equivalentTo)
- EFO:1000408 (MONDO:equivalentTo)
- UMLS:C1266128 (NCIT:C6582)
- ICDO:8842/0 (NCIT:C6582)
- NCIT:C6582 (MONDO:equivalentTo)
- DOID:2685 (MONDO:equivalentTo)
- ONCOTREE:OFMT (MONDO:equivalentTo)
A rare soft tissue tumor of uncertain lineage characterized by the presence of neoplastic spindle to round cells forming cords in a fibromyxoid stroma. The lesions are associated with the formation of metaplastic bone. Most patients present with painless subcutaneous masses. Recurrences have been reported in a minority of patients.
http://purl.obolibrary.org/obo/DOID_2685, http://identifiers.org/snomedct/404076001, http://purl.obolibrary.org/obo/NCIT_C6582, http://linkedlifedata.com/resource/umls/id/C1266128
http://purl.obolibrary.org/obo/MONDO_0002616
ossifying fibromyxoma, ossifying fibromyxoid neoplasm, OFMT, ossifying fibromyxoid tumor (morphologic abnormality)
MONDO:0006330