Malignant mesenchymal neoplasms

Тодорхойлолт

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.

Дэд ангилал 20

• 2B50Chondrosarcoma, primary site›
• 2B51Osteosarcoma, primary site›
• 2B52Ewing sarcoma, primary site›
• 2B53Fibroblastic or myofibroblastic tumour, primary site›
• 2B54Unclassified pleomorphic sarcoma, primary site›
• 2B55Rhabdomyosarcoma, primary site›
• 2B56Angiosarcoma, primary site›
• 2B57Kaposi sarcoma, primary site›
• 2B58Leiomyosarcoma, primary site›
• 2B59Liposarcoma, primary site›
• 2B5ASynovial sarcoma, primary site›
• 2B5BGastrointestinal stromal tumour, primary site›
• 2B5CEndometrial stromal sarcoma, primary site›
• 2B5DMalignant mixed epithelial mesenchymal tumour, primary site›
• 2B5EMalignant nerve sheath tumour of peripheral nerves or autonomic nervous system, primary site›
• 2B5FSarcoma, not elsewhere classified, primary site›
• 2B5GMyosarcoma of uterus, part not specified›
• 2B5HWell differentiated lipomatous tumour, primary site›
• 2B5JMalignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites›
• 2B5KUnspecified malignant soft tissue tumours or sarcomas of bone or articular cartilage of other or unspecified sites›