Extraskeletal Ewing's sarcoma: prolonged survival with recurrence after operation
Unlike the osseous variety, extraskeletal small cell tumors histologically identical to Ewing's sarcoma of bone frequently respond to radical surgical excision. The relative infrequence of this tumor, compounded by the comprehensive eponym "Ewing's sarcoma," may deter surgical in...
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Veröffentlicht in: | Southern medical journal (Birmingham, Ala.) Ala.), 1980-09, Vol.73 (9), p.1294-1295 |
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creator | Covelli, H D Beekman, J F Kingry, R L |
description | Unlike the osseous variety, extraskeletal small cell tumors histologically identical to Ewing's sarcoma of bone frequently respond to radical surgical excision. The relative infrequence of this tumor, compounded by the comprehensive eponym "Ewing's sarcoma," may deter surgical intervention in this group of patients. This patient's course demonstrates the value of surgery alone, but emphasizes the role of combined surgery, irradiation, and chemotherapy as the best management for extraskeletal Ewing's sarcoma. |
doi_str_mv | 10.1097/00007611-198009000-00053 |
format | Article |
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The relative infrequence of this tumor, compounded by the comprehensive eponym "Ewing's sarcoma," may deter surgical intervention in this group of patients. This patient's course demonstrates the value of surgery alone, but emphasizes the role of combined surgery, irradiation, and chemotherapy as the best management for extraskeletal Ewing's sarcoma.</description><identifier>ISSN: 0038-4348</identifier><identifier>DOI: 10.1097/00007611-198009000-00053</identifier><identifier>PMID: 7414394</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Female ; Humans ; Neoplasm Recurrence, Local ; Sarcoma, Ewing - surgery ; Soft Tissue Neoplasms - surgery ; Thoracic Neoplasms - surgery</subject><ispartof>Southern medical journal (Birmingham, Ala.), 1980-09, Vol.73 (9), p.1294-1295</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7414394$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Covelli, H D</creatorcontrib><creatorcontrib>Beekman, J F</creatorcontrib><creatorcontrib>Kingry, R L</creatorcontrib><title>Extraskeletal Ewing's sarcoma: prolonged survival with recurrence after operation</title><title>Southern medical journal (Birmingham, Ala.)</title><addtitle>South Med J</addtitle><description>Unlike the osseous variety, extraskeletal small cell tumors histologically identical to Ewing's sarcoma of bone frequently respond to radical surgical excision. The relative infrequence of this tumor, compounded by the comprehensive eponym "Ewing's sarcoma," may deter surgical intervention in this group of patients. This patient's course demonstrates the value of surgery alone, but emphasizes the role of combined surgery, irradiation, and chemotherapy as the best management for extraskeletal Ewing's sarcoma.</description><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Neoplasm Recurrence, Local</subject><subject>Sarcoma, Ewing - surgery</subject><subject>Soft Tissue Neoplasms - surgery</subject><subject>Thoracic Neoplasms - surgery</subject><issn>0038-4348</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1PwzAMhnMAjTH4CUg5wamQNEmTcEPT-JAmISQ4R2nmjkLbjKTd4N-TsTFLlmXptf36QQhTck2JljckhSwozahWhOjUZSkFO0JjQpjKOOPqBJ3G-LEVClWM0EhyypnmY_Qy--6DjZ_QQG8bPNvU3fIq4miD8629xavgG98tYYHjENb1Omk2df-OA7ghBOgcYFv1ELBfQbB97bszdFzZJsL5vk7Q2_3sdfqYzZ8fnqZ388zlQvRZbq1gHEBInleKqlLqkkqhrbAMCtDppaJkxCWnjGkhy6JQFVFECc6JBsIm6HK3N1n8GiD2pq2jg6axHfghGilyUaTlSah2Qhd8jAEqswp1a8OPocRsCZp_guZA0PwRTKMX-xtD2cLiMLjHx34B7HptaQ</recordid><startdate>198009</startdate><enddate>198009</enddate><creator>Covelli, H D</creator><creator>Beekman, J F</creator><creator>Kingry, R L</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198009</creationdate><title>Extraskeletal Ewing's sarcoma: prolonged survival with recurrence after operation</title><author>Covelli, H D ; Beekman, J F ; Kingry, R L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c255t-2aa534ee5742f818b79b1759a5a3e6e90766b30c74133957b668f080854409e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Adult</topic><topic>Female</topic><topic>Humans</topic><topic>Neoplasm Recurrence, Local</topic><topic>Sarcoma, Ewing - surgery</topic><topic>Soft Tissue Neoplasms - surgery</topic><topic>Thoracic Neoplasms - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Covelli, H D</creatorcontrib><creatorcontrib>Beekman, J F</creatorcontrib><creatorcontrib>Kingry, R L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Southern medical journal (Birmingham, Ala.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Covelli, H D</au><au>Beekman, J F</au><au>Kingry, R L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extraskeletal Ewing's sarcoma: prolonged survival with recurrence after operation</atitle><jtitle>Southern medical journal (Birmingham, Ala.)</jtitle><addtitle>South Med J</addtitle><date>1980-09</date><risdate>1980</risdate><volume>73</volume><issue>9</issue><spage>1294</spage><epage>1295</epage><pages>1294-1295</pages><issn>0038-4348</issn><abstract>Unlike the osseous variety, extraskeletal small cell tumors histologically identical to Ewing's sarcoma of bone frequently respond to radical surgical excision. The relative infrequence of this tumor, compounded by the comprehensive eponym "Ewing's sarcoma," may deter surgical intervention in this group of patients. This patient's course demonstrates the value of surgery alone, but emphasizes the role of combined surgery, irradiation, and chemotherapy as the best management for extraskeletal Ewing's sarcoma.</abstract><cop>United States</cop><pmid>7414394</pmid><doi>10.1097/00007611-198009000-00053</doi><tpages>2</tpages></addata></record> |
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ispartof | Southern medical journal (Birmingham, Ala.), 1980-09, Vol.73 (9), p.1294-1295 |
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source | MEDLINE; Journals@Ovid Complete |
subjects | Adult Female Humans Neoplasm Recurrence, Local Sarcoma, Ewing - surgery Soft Tissue Neoplasms - surgery Thoracic Neoplasms - surgery |
title | Extraskeletal Ewing's sarcoma: prolonged survival with recurrence after operation |
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