ADULT SOFT TISSUE SARCOMA
Identifieur interne : 003873 ( Istex/Checkpoint ); précédent : 003872; suivant : 003874ADULT SOFT TISSUE SARCOMA
Auteurs : G. Bruce Mann ; Jonathan J. Lewis [États-Unis] ; Murray F. Brennan [États-Unis]Source :
- Australian and New Zealand Journal of Surgery [ 0004-8682 ] ; 1999-05.
Abstract
Background: Soft tissue sarcomas (STS) are a group of anatomically and histologically diverse tumours. They account for about 1% of adult malignancies, and about 50% of patients diagnosed with sarcoma eventually die of the disease. These tumours are grouped together because of shared biological characteristics and treatment responses.
Url:
DOI: 10.1046/j.1440-1622.1999.01568.x
Affiliations:
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ISTEX:528184A920D1F5BC5B449D518BE19722F9228128Le document en format XML
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<front><div type="abstract">Background: Soft tissue sarcomas (STS) are a group of anatomically and histologically diverse tumours. They account for about 1% of adult malignancies, and about 50% of patients diagnosed with sarcoma eventually die of the disease. These tumours are grouped together because of shared biological characteristics and treatment responses.</div>
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