Structured Summary
Abstract
A rare aggressive variant of chondrosarcoma, characterized by a biphasic histologic pattern of small compact cells intermixed with islands of cartilaginous matrix. Mesenchymal chondrosarcomas have a predilection for flat bones; long tubular bones are rarely affected. They tend to occur in the younger age group and are highly metastatic. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1456)
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Classification
Broader headings
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Synonyms
3 entry terms
- Chondrosarcoma, Mesenchymal
- Chondrosarcomas, Mesenchymal
- Mesenchymal Chondrosarcomas
MeSH Record
Aspects Covered
39 allowable subheadings
Indexed with the subheadings blood, blood supply, cerebrospinal fluid, chemically induced, chemistry, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, secondary, surgery, therapy, ultrastructure, urine, veterinary, virology.
MeSH Record
Indexing Annotation
coordinate with BONE NEOPLASMS or specific precoordinated bone/neoplasm term or specific bone + BONE NEOPLASMS
MeSH Record
History Note
94
MeSH Record
Previous Indexing
- Chondrosarcoma (1966-1993)
- Mesenchymoma (1966-1991)
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Mesenchymal Chondrosarcoma. Medical Subject Headings (MeSH). 2026. Unique ID D018211. http://id.nlm.nih.gov/mesh/2026/D018211
- Mesenchymal Chondrosarcoma. In: Wikipedia. https://en.wikipedia.org/wiki/Mesenchymal_chondrosarcoma
- Mesenchymal Chondrosarcoma. In: Wikidata. https://www.wikidata.org/wiki/Q6821200