Malignant mesenchymal neoplasms
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A usually aggressive malignant mesenchymal cell tumour most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The prognosis depends largely on the degree of differentiation (grade) of the tumour. Representative subtypes are liposarcoma, leiomyosarcoma, osteosarcoma, and chondrosarcoma.
exclusions
sections/codes in this section (2B50-2B5Z)
- Chondrosarcoma, primary site (2B50)
- Osteosarcoma, primary site (2B51)
- Ewing sarcoma, primary site (2B52)
- Fibroblastic or myofibroblastic tumour, primary site (2B53)
- Unclassified pleomorphic sarcoma, primary site (2B54)
- Rhabdomyosarcoma, primary site (2B55)
- Angiosarcoma, primary site (2B56)
- Kaposi sarcoma, primary site (2B57)
- Leiomyosarcoma, primary site (2B58)
- Liposarcoma, primary site (2B59)
- Synovial sarcoma, primary site (2B5A)
- Gastrointestinal stromal tumour, primary site (2B5B)
- Endometrial stromal sarcoma, primary site (2B5C)
- Malignant mixed epithelial mesenchymal tumour, primary site (2B5D)
- Malignant nerve sheath tumour of peripheral nerves or autonomic nervous system, primary site (2B5E)
- Sarcoma, not elsewhere classified, primary site (2B5F)
- Myosarcoma of uterus, part not specified (2B5G)
- Well differentiated lipomatous tumour, primary site (2B5H)
- Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites (2B5J)
- Unspecified malignant soft tissue tumours or sarcomas of bone or articular cartilage of other or unspecified sites (2B5K)
- Other specified malignant mesenchymal neoplasms (2B5Y)
- Malignant mesenchymal neoplasm of unspecified type (2B5Z)
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