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Surgical management and outcomes of spinal clear cell sarcoma: A retrospective study of five cases and literature review
Abstract Purpose Clear cell sarcoma (CCS) is a rare high-grade malignant tumor accounting for less than 1% of all soft tissue sarcomas. CCS in the spine is much rarer and poorly understood. The objective of our study is to discuss clinical characteristics, surgical management and outcomes of spinal...
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Published in: | Journal of bone oncology 2017-03, Vol.6 (C), p.27-31 |
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creator | Gao, Xin Zhao, Chenglong Wang, Jing Cai, Xiaopan Chen, Guanghui Liu, Weibo Zou, Weiwei He, Jin Xiao, Jianru Liu, Tielong |
description | Abstract Purpose Clear cell sarcoma (CCS) is a rare high-grade malignant tumor accounting for less than 1% of all soft tissue sarcomas. CCS in the spine is much rarer and poorly understood. The objective of our study is to discuss clinical characteristics, surgical management and outcomes of spinal CCS. Methods Between October 2011 and December 2014, five patients with spinal CCS underwent surgical treatment in our center. Five cases from literature focusing on the spinal CCS were also reviewed. We retrospectively analyzed clinical data and outcome of all ten patients to present our understanding of spinal CCS. Results Three en bloc and two piecemeal resections were performed successfully. The syndromes of all the patients were obviously relieved after operation. The mean follow-up period was 24.4 months (range 10–41 months). Two patients died of lung metastasis 10 and 26 months after operation respectively. One patient was alive with tumor recurrence. Other two patients were alive with no evidence of disease at last follow-up. Conclusions Prognosis of spinal CCS tend to be worse than CCS in common sites. En bloc resection could be regarded as the first treatment option. Tumor size, tumor location, preoperative neurological status and resection mode might be the potential prognostic factors of spinal CCS. |
doi_str_mv | 10.1016/j.jbo.2016.09.002 |
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CCS in the spine is much rarer and poorly understood. The objective of our study is to discuss clinical characteristics, surgical management and outcomes of spinal CCS. Methods Between October 2011 and December 2014, five patients with spinal CCS underwent surgical treatment in our center. Five cases from literature focusing on the spinal CCS were also reviewed. We retrospectively analyzed clinical data and outcome of all ten patients to present our understanding of spinal CCS. Results Three en bloc and two piecemeal resections were performed successfully. The syndromes of all the patients were obviously relieved after operation. The mean follow-up period was 24.4 months (range 10–41 months). Two patients died of lung metastasis 10 and 26 months after operation respectively. One patient was alive with tumor recurrence. Other two patients were alive with no evidence of disease at last follow-up. Conclusions Prognosis of spinal CCS tend to be worse than CCS in common sites. En bloc resection could be regarded as the first treatment option. Tumor size, tumor location, preoperative neurological status and resection mode might be the potential prognostic factors of spinal CCS.</description><identifier>ISSN: 2212-1374</identifier><identifier>EISSN: 2212-1374</identifier><identifier>DOI: 10.1016/j.jbo.2016.09.002</identifier><language>eng</language><publisher>Elsevier GmbH</publisher><subject>Clear cell sarcoma ; Hematology, Oncology and Palliative Medicine ; Prognostic factors ; Spine ; Surgery</subject><ispartof>Journal of bone oncology, 2017-03, Vol.6 (C), p.27-31</ispartof><rights>2016 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-f323c195501fb5ba58ad434535ae4ced9c3a75d47a4e9918f44b3986e08fa84a3</citedby><cites>FETCH-LOGICAL-c461t-f323c195501fb5ba58ad434535ae4ced9c3a75d47a4e9918f44b3986e08fa84a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2212137416300483$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids></links><search><creatorcontrib>Gao, Xin</creatorcontrib><creatorcontrib>Zhao, Chenglong</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Cai, Xiaopan</creatorcontrib><creatorcontrib>Chen, Guanghui</creatorcontrib><creatorcontrib>Liu, Weibo</creatorcontrib><creatorcontrib>Zou, Weiwei</creatorcontrib><creatorcontrib>He, Jin</creatorcontrib><creatorcontrib>Xiao, Jianru</creatorcontrib><creatorcontrib>Liu, Tielong</creatorcontrib><title>Surgical management and outcomes of spinal clear cell sarcoma: A retrospective study of five cases and literature review</title><title>Journal of bone oncology</title><description>Abstract Purpose Clear cell sarcoma (CCS) is a rare high-grade malignant tumor accounting for less than 1% of all soft tissue sarcomas. CCS in the spine is much rarer and poorly understood. The objective of our study is to discuss clinical characteristics, surgical management and outcomes of spinal CCS. Methods Between October 2011 and December 2014, five patients with spinal CCS underwent surgical treatment in our center. Five cases from literature focusing on the spinal CCS were also reviewed. We retrospectively analyzed clinical data and outcome of all ten patients to present our understanding of spinal CCS. Results Three en bloc and two piecemeal resections were performed successfully. The syndromes of all the patients were obviously relieved after operation. The mean follow-up period was 24.4 months (range 10–41 months). Two patients died of lung metastasis 10 and 26 months after operation respectively. One patient was alive with tumor recurrence. Other two patients were alive with no evidence of disease at last follow-up. Conclusions Prognosis of spinal CCS tend to be worse than CCS in common sites. En bloc resection could be regarded as the first treatment option. Tumor size, tumor location, preoperative neurological status and resection mode might be the potential prognostic factors of spinal CCS.</description><subject>Clear cell sarcoma</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Prognostic factors</subject><subject>Spine</subject><subject>Surgery</subject><issn>2212-1374</issn><issn>2212-1374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kdGO1CAUhhujiZvdfQDveIGpUGgLmphsNrpusokXq9fklB4m1E6ZAF2dt_fUMWbjhdxwDvD_8PNV1RvBa8FF93aqpyHWDZU1NzXnzYvqomlEsxOyVy-f1a-r65wnTqMXsunNRfXzcU374GBmB1hgjwdcCoNlZHEtLh4ws-hZPoaFTrgZITGH88wyJNqFd-yGJSwp5iO6Ep6Q5bKOp03jt85BJofNbg4FE5Q1IQmeAv64ql55mDNe_5kvq2-fPn69_bx7-HJ3f3vzsHOqE2XnZSOdMG3LhR_aAVoNo5KqlS2gcjgaJ6FvR9WDQmOE9koN0ugOufagFcjL6v7sO0aY7DGFA6STjRDs74WY9hZSCZTN6oGu0uQxdKiQyg6x5741RlKvOXmJs5ejxDmh_-snuN1I2MkSCbuRsNxYIkGa92cNUkgKnmx2ARd6ekj0Z_SK8F_1h3_Ubg7Lxus7njBPcU1EJlthc2O5fdxIb6BFJzlXWspfnlWnMQ</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Gao, Xin</creator><creator>Zhao, Chenglong</creator><creator>Wang, Jing</creator><creator>Cai, Xiaopan</creator><creator>Chen, Guanghui</creator><creator>Liu, Weibo</creator><creator>Zou, Weiwei</creator><creator>He, Jin</creator><creator>Xiao, Jianru</creator><creator>Liu, Tielong</creator><general>Elsevier GmbH</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>20170301</creationdate><title>Surgical management and outcomes of spinal clear cell sarcoma: A retrospective study of five cases and literature review</title><author>Gao, Xin ; Zhao, Chenglong ; Wang, Jing ; Cai, Xiaopan ; Chen, Guanghui ; Liu, Weibo ; Zou, Weiwei ; He, Jin ; Xiao, Jianru ; Liu, Tielong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-f323c195501fb5ba58ad434535ae4ced9c3a75d47a4e9918f44b3986e08fa84a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Clear cell sarcoma</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Prognostic factors</topic><topic>Spine</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Xin</creatorcontrib><creatorcontrib>Zhao, Chenglong</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Cai, Xiaopan</creatorcontrib><creatorcontrib>Chen, Guanghui</creatorcontrib><creatorcontrib>Liu, Weibo</creatorcontrib><creatorcontrib>Zou, Weiwei</creatorcontrib><creatorcontrib>He, Jin</creatorcontrib><creatorcontrib>Xiao, Jianru</creatorcontrib><creatorcontrib>Liu, Tielong</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of bone oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Xin</au><au>Zhao, Chenglong</au><au>Wang, Jing</au><au>Cai, Xiaopan</au><au>Chen, Guanghui</au><au>Liu, Weibo</au><au>Zou, Weiwei</au><au>He, Jin</au><au>Xiao, Jianru</au><au>Liu, Tielong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surgical management and outcomes of spinal clear cell sarcoma: A retrospective study of five cases and literature review</atitle><jtitle>Journal of bone oncology</jtitle><date>2017-03-01</date><risdate>2017</risdate><volume>6</volume><issue>C</issue><spage>27</spage><epage>31</epage><pages>27-31</pages><issn>2212-1374</issn><eissn>2212-1374</eissn><abstract>Abstract Purpose Clear cell sarcoma (CCS) is a rare high-grade malignant tumor accounting for less than 1% of all soft tissue sarcomas. CCS in the spine is much rarer and poorly understood. The objective of our study is to discuss clinical characteristics, surgical management and outcomes of spinal CCS. Methods Between October 2011 and December 2014, five patients with spinal CCS underwent surgical treatment in our center. Five cases from literature focusing on the spinal CCS were also reviewed. We retrospectively analyzed clinical data and outcome of all ten patients to present our understanding of spinal CCS. Results Three en bloc and two piecemeal resections were performed successfully. The syndromes of all the patients were obviously relieved after operation. The mean follow-up period was 24.4 months (range 10–41 months). Two patients died of lung metastasis 10 and 26 months after operation respectively. One patient was alive with tumor recurrence. Other two patients were alive with no evidence of disease at last follow-up. Conclusions Prognosis of spinal CCS tend to be worse than CCS in common sites. En bloc resection could be regarded as the first treatment option. Tumor size, tumor location, preoperative neurological status and resection mode might be the potential prognostic factors of spinal CCS.</abstract><pub>Elsevier GmbH</pub><doi>10.1016/j.jbo.2016.09.002</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Clear cell sarcoma Hematology, Oncology and Palliative Medicine Prognostic factors Spine Surgery |
title | Surgical management and outcomes of spinal clear cell sarcoma: A retrospective study of five cases and literature review |
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