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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1987-2-13
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pubmed:abstractText |
Mesenchymal chondrosarcoma is a rare tumor distinctly different from the more common chondrosarcoma. It shows a predilection for the head and neck in both osseous and extraosseous forms. The prognosis for cure is poor, with a high incidence of local recurrence as well as regional and distant metastasis. Treatment is based on radical surgical excision, although combination chemo-therapy has recently shown promise. Additional experience with this tumor is required to define the most efficacious form of treatment.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
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pubmed:month |
Jan
|
pubmed:issn |
0278-2391
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
45
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
72-5
|
pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:3467042-Adult,
pubmed-meshheading:3467042-Chondrosarcoma,
pubmed-meshheading:3467042-Diagnosis, Differential,
pubmed-meshheading:3467042-Humans,
pubmed-meshheading:3467042-Male,
pubmed-meshheading:3467042-Mandibular Neoplasms,
pubmed-meshheading:3467042-Neoplasm Metastasis,
pubmed-meshheading:3467042-Sarcoma, Ewing
|
pubmed:year |
1987
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pubmed:articleTitle |
Mesenchymal chondrosarcoma: a case report.
|
pubmed:publicationType |
Journal Article,
Case Reports
|