Management of extremity soft tissue sarcomas
Identifieur interne : 004A45 ( Pmc/Curation ); précédent : 004A44; suivant : 004A46Management of extremity soft tissue sarcomas
Auteurs : Ajay Puri [Inde] ; Ashish Gulia [Inde]Source :
- Indian Journal of Orthopaedics [ 0019-5413 ] ; 2011.
Abstract
Soft-tissue sarcomas are a rare and heterogeneous group of tumors. The last few decades have seen rapid strides in surgery with function preserving alternatives for local control in these lesions becoming the norm without compromising on overall disease survival. Good functional and oncological results can be achieved with a combination of excision of the tumor, and where required, suitable adjuvant therapies. These lesions are best managed at specialty centres where the requisite multidisciplinary care can be offered to the patient to optimise results. This overview is intended as a review of current understanding and the multimodality management of these challenging tumors.
Url:
DOI: 10.4103/0019-5413.82332
PubMed: 21772621
PubMed Central: 3134013
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<front><div type="abstract" xml:lang="en"><p>Soft-tissue sarcomas are a rare and heterogeneous group of tumors. The last few decades have seen rapid strides in surgery with function preserving alternatives for local control in these lesions becoming the norm without compromising on overall disease survival. Good functional and oncological results can be achieved with a combination of excision of the tumor, and where required, suitable adjuvant therapies. These lesions are best managed at specialty centres where the requisite multidisciplinary care can be offered to the patient to optimise results. This overview is intended as a review of current understanding and the multimodality management of these challenging tumors.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Indian J Orthop</journal-id>
<journal-id journal-id-type="publisher-id">IJOrtho</journal-id>
<journal-title-group><journal-title>Indian Journal of Orthopaedics</journal-title>
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<issn pub-type="ppub">0019-5413</issn>
<issn pub-type="epub">1998-3727</issn>
<publisher><publisher-name>Medknow Publications Pvt Ltd</publisher-name>
<publisher-loc>India</publisher-loc>
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<article-meta><article-id pub-id-type="pmid">21772621</article-id>
<article-id pub-id-type="pmc">3134013</article-id>
<article-id pub-id-type="publisher-id">IJOrtho-45-301</article-id>
<article-id pub-id-type="doi">10.4103/0019-5413.82332</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Review Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Management of extremity soft tissue sarcomas</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Puri</surname>
<given-names>Ajay</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
<xref ref-type="corresp" rid="cor1"></xref>
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<contrib contrib-type="author"><name><surname>Gulia</surname>
<given-names>Ashish</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
</contrib>
</contrib-group>
<aff id="aff1">Department of Orthopaedic Oncology, Tata Memorial Hospital, Mumbai, India</aff>
<author-notes><corresp id="cor1"><bold>Address for correspondence:</bold>
Prof. Ajay Puri, Room No: 26, Tata Memorial Hospital, E. Borges Road, Parel, Mumbai-400 012, India. E-mail: <email xlink:href="docpuri@gmail.com">docpuri@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub"><season>Jul-Aug</season>
<year>2011</year>
</pub-date>
<volume>45</volume>
<issue>4</issue>
<fpage>301</fpage>
<lpage>306</lpage>
<permissions><copyright-statement>© Indian Journal of Orthopaedics</copyright-statement>
<copyright-year>2011</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract><p>Soft-tissue sarcomas are a rare and heterogeneous group of tumors. The last few decades have seen rapid strides in surgery with function preserving alternatives for local control in these lesions becoming the norm without compromising on overall disease survival. Good functional and oncological results can be achieved with a combination of excision of the tumor, and where required, suitable adjuvant therapies. These lesions are best managed at specialty centres where the requisite multidisciplinary care can be offered to the patient to optimise results. This overview is intended as a review of current understanding and the multimodality management of these challenging tumors.</p>
</abstract>
<kwd-group><kwd>Limb salvage</kwd>
<kwd>multidisciplinary care</kwd>
<kwd>soft tissue sarcoma</kwd>
</kwd-group>
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