Central nervous system mesenchymal non-meningothelial tumor

Definition

A benign or malignant mesenchymal neoplasm originating in the central nervous system or the meninges and showing fibrous, fibrohistiocytic, adipose, myoid, endothelial, chondroid or osseous, but not meningothelial differentiation. Depending on the histological features and clinical behavior of these neoplasms, their grade ranges from benign (WHO grade I) to highly malignant (WHO grade IV). (Adapted from WHO)

Also known as central nervous system mesenchymal, non-meningothelial neoplasm, central nervous system mesenchymal, non-meningothelial tumor, central nervous system mesenchymal, non-meningothelial tumour, central nervous system soft tissue neoplasm, central nervous system soft tissue tumor, central nervous system soft tissue tumour, CNS soft tissue neoplasm, CNS soft tissue tumor, CNS soft tissue tumour, mesenchymal non-meningothelial tumor of the central nervous system, mesenchymal non-meningothelial tumour of the central nervous system, mesenchymal, non-meningothelial tumor of central nervous system, mesenchymal, non-meningothelial tumor of CNS, mesenchymal, non-meningothelial tumor of the CNS, mesenchymal, non-meningothelial tumour of central nervous system, mesenchymal, non-meningothelial tumour of CNS, mesenchymal, non-meningothelial tumour of the CNS, soft tissue neoplasm of central nervous system, soft tissue neoplasm of CNS, soft tissue neoplasm of the central nervous system, soft tissue neoplasm of the CNS, soft tissue tumor of central nervous system, soft tissue tumor of CNS, soft tissue tumor of the central nervous system, soft tissue tumor of the CNS, soft tissue tumour of central nervous system, soft tissue tumour of CNS, soft tissue tumour of the central nervous system, soft tissue tumour of the CNS — per MONDO

Also identified as

• DOID 502 per MONDO
• NCIT C5449 per MONDO
• UMLS C1332893 per MONDO

Affected Organs