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Chordoma is a rare slow-growing neoplasm thought to arise from cellular remnants of the notochord.The evidence for this is the location of the tumors (along the neuraxis), the similar immunohistochemical staining patterns, and the demonstration that notochordal cells are preferentially left behind in the clivus and sacrococcygeal regions when the remainder of the notochord regresses during ...
Europe and other parts of the world use the ICD-10. The root codes for ICD-10 and ICD-10-CM are the same, making it helpful for locating codes for general body systems and disease processes. [2] [3] In ICD-11 the search and coding of any disease, including rare ones is done via the ICD-11 website. [4]
M9221/3 Juxtacortical chondrosarcoma Periosteal chondrosarcoma; M9230/0 Chondroblastoma, NOS Chondromatous giant cell tumor; Codman tumor; M9230/3 Chondroblastoma, malignant M9231/3 Myxoid chondrosarcoma M9240/3 Mesenchymal chondrosarcoma M9241/0 Chondromyxoid fibroma M9242/3 Clear cell chondrosarcoma M9243/3 Dedifferentiated chondrosarcoma
Chondrosarcoma is a bone sarcoma, a primary cancer composed of cells derived from transformed cells that produce cartilage. [1] A chondrosarcoma is a member of a category of tumors of bone and soft tissue known as sarcomas .
10–19 Muscle (smooth) Leiomyosarcoma Trunk 15-35+ Fibrous tissue Undifferentiated pleomorphic sarcoma Legs 15–19+ Dermatofibrosarcoma protuberans Trunk 15–19 Synovial sarcoma Legs, arms, and trunk 15–35 Fat Liposarcoma Arms and Legs 15–19+ Peripheral nerves Malignant peripheral nerve sheath tumors (also called neurofibrosarcomas)
EMC was firstly described in 1953 by Stout et al. when they discussed the different species of extraskeletal chondrosarcoma, [2] but EMC concept was firstly proposed in 1972 by Enzinger et al. [3] Brody thought that this was a unique low-grade malignancy with a low growth rate and both clinically and histopathologically distinct anamnesis beside the typical chondrosarcomas. [4]
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]
[3] It is generally considered to be a disease of childhood, as the vast majority of cases occur in those below the age of 18. It is commonly described as one of the small-blue-round-cell tumors of childhood due to its appearance on an H&E stain. [4] Despite being relatively rare, it accounts for approximately 40% of all recorded soft-tissue ...