Descriptor English: | Chondroblastoma | ||||
Descriptor Spanish: |
Condroblastoma
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Descriptor Portuguese: | Condroblastoma | ||||
Descriptor French: | Chondroblastome | ||||
Entry term(s): |
Chondroblastomas |
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Tree number(s): |
C04.557.450.565.250 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D002804 | ||||
Scope note: | A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846) |
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Annotation: | benign or malignant; coordinate with BONE NEOPLASMS or precoordinated organ/neoplasm term |
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Allowable Qualifiers: |
BL blood BS blood supply CF cerebrospinal fluid CH chemistry CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SC secondary SU surgery TH therapy UL ultrastructure UR urine VE veterinary VI virology |
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DeCS ID: | 2854 | ||||
Unique ID: | D002804 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1966/01/01 | ||||
Date of Entry: | 1999/01/01 | ||||
Revision Date: | 1995/06/08 |
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DISEASES
Neoplasms [C04]Neoplasms
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Chondroblastoma
- Preferred
Concept UI |
M0004304 |
Scope note | A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846) |
Preferred term | Chondroblastoma |
Entry term(s) |
Chondroblastomas |
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