chondrosarcoma


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Related to chondrosarcoma: osteosarcoma, mesenchymal chondrosarcoma

chondrosarcoma

 [kon″dro-sahr-ko´ma]
a malignant tumor derived from cartilage cells or their precursors.

chon·dro·sar·co·ma

(kon'drō-sar-kō'mă), [MIM*215300]
A malignant neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, in middle-aged and older people; most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion.

chondrosarcoma

/chon·dro·sar·co·ma/ (-sar-ko´ma) a malignant tumor derived from cartilage cells or their precursors.
central chondrosarcoma  one within a bone, usually not associated with a mass.

chondrosarcoma

[kon′drōsärkō′mə] pl. chondrosarcomas, chondrosarcomata
Etymology: Gk, chondros + sarx, flesh, oma, tumor
a malignant neoplasm of cartilaginous cells or their precursors that occurs most frequently in long bones, the pelvic girdle, and the scapula. The tumor is a large, smooth, lobulated growth composed of nodules of hyaline cartilage that may show slight to marked calcification. Also called chondroma sarcomatosum. chondrosarcomatous, adj.
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Chondrosarcoma

chondrosarcoma

A malignant mesenchymal tumour caused by the uncontrolled proliferation of chondroblasts. It is the second most common primary malignancy of bone after osteosarcoma and represents 25% of such lesions.

Epidemiology
Arise in the axial and proximal skeleton of adults and older people.

Clinical findings
Often asyptomatic initially; later, pain for months to years, swelling.

Imaging
MRI is the modality of choice; CT, plain films, show destructive, aggressive permeation of diaphysis by tumour.
 
DiffDx
Metastatic carcinoma, enchondroma, chondromyxoid fibroma.

Types
Clear cell, de-differented, extraskeletal mesenchymal, juxtacortical, mesenchymal, myxoid.

Prognosis
Grade 1, 88% 5-year survival; grade 3, 40% 5-year survival.

chon·dro·sar·co·ma

(kon'drō-sahr-kō'mă)
A malignant neoplasm derived from cartilage cells.

chondrosarcoma

A rare malignant tumour of the cartilaginous parts of bone affecting mainly the pelvis, ribs and breastbone (sternum) and causes a slowly expanding swelling. The outlook after surgical removal is usually favourable.

chon·dro·sar·co·ma

(kon'drō-sahr-kō'mă) [MIM*215300]
A malignant neoplasm derived from cartilage cells.

chondrosarcoma

a malignant tumor derived from cartilage cells or their precursors.
References in periodicals archive ?
Jux tacortical chondrosarcoma of the mandible: Report of a unique case and review of the literature.
Isocitrate dehydrogenase (IDH)1 and IDH2 mutations characterize cartilaginous tumors such as enchondromas and chondrosarcomas, but are absent in CBT.
The postoperative pathologic examination was reported as grade 1, well-differentiated chondrosarcoma (Figure 3).
The cartilage tumour has surrounded the normal trabeculae, producing a cartilage matrix with increased cellularity and enlarged nuclei, typical of chondrosarcoma.
The report reviews pipeline therapeutics for Chondrosarcoma by companies and universities/research institutes based on information derived from company and industry-specific sources
Hopper, "Spinal chondrosarcoma arising from a solitary lumbar osteochondroma," Journal of the Belgian Society of Radiology, vol.
An increase in the thickness of the cartilaginous cap of more than 1 cm (visible on an x-ray) should raise the suspicion of chondrosarcoma (6).
The report reviews key players involved in the therapeutics development for Chondrosarcoma and enlists all their major and minor projects
OUMS-27 cell lines that have been established from chondrosarcoma cells and express chondrocytic properties are used in investigating pathophysiology of cartilage disorders due to the difficulties in obtaining chondrocytes.
There are no reports of chondrosarcoma in parrots and few descriptions in other bird species, such as ruffed grouse (Bonasa umbellus) (SIEGFRIED, 1983), great egret (Ardea herodius occidentalis and Ardea alba) (SPALDING & WOODARD, 1992; KUBO et al.
4) Chondroid bladder tumours are very rare, with only 2 reported cases of soft tissue chondroma, (1,2) and 5 of chondrosarcoma.
Cases of malignant transformation to chondrosarcoma have also been reported, but such an outcome is very rare [5, 6].