Initial and Long-term Results in the Management of Primary Chest Wall Neoplasms
One hundred ten patients with primary chest wall neoplasms were analyzed for long-term results. The diagnosis of 59 malignant and 51 benign tumors was confirmed by the Armed Forces Institute of Pathology. No deaths were associated with primary definitive therapy. Among the five most frequently encou...
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Veröffentlicht in: | The Annals of thoracic surgery 1982-12, Vol.34 (6), p.664-673 |
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container_title | The Annals of thoracic surgery |
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creator | Graeber, Geoffrey M. Snyder, Robert J. Fleming, Arthur W. Head, Harold D. Lough, Frederick C. Parker, John S. Zajtchuk, Rostik Brott, Walter H. |
description | One hundred ten patients with primary chest wall neoplasms were analyzed for long-term results. The diagnosis of 59 malignant and 51 benign tumors was confirmed by the Armed Forces Institute of Pathology. No deaths were associated with primary definitive therapy. Among the five most frequently encountered malignant tumor types, five-year survivals were obtained in 9 of 17 (53%) patients with fibrosarcoma, 8 of 9 (89%) patients with chondrosarcoma, 2 of 8 (25%) patients with solitary chest wall plasmacytoma (multiple myeloma), 1 of 6 (17%) patients with Ewing's sarcoma, and 2 of 4 (50%) of patients with osteogenic sarcoma. Although the five-year survival appears to indicate therapeutic success in patients with Ewing's sarcoma and osteogenic sarcoma, patients with chondrosarcoma or fibrosarcoma may have a more protracted course, and those with solitary plasmacytoma usually develop multiple myeloma. The findings suggest that radical surgical excision is the treatment of choice for chondrosarcoma; radical surgical excision combined with chemotherapy, for fibrosarcoma and osteogenic sarcoma; surgical excision combined with radiation and chemotherapy, for Ewing's sarcoma; and systemic surveillance and therapy, for pathologically confirmed solitary plasmacytoma. |
doi_str_mv | 10.1016/S0003-4975(10)60906-X |
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The diagnosis of 59 malignant and 51 benign tumors was confirmed by the Armed Forces Institute of Pathology. No deaths were associated with primary definitive therapy. Among the five most frequently encountered malignant tumor types, five-year survivals were obtained in 9 of 17 (53%) patients with fibrosarcoma, 8 of 9 (89%) patients with chondrosarcoma, 2 of 8 (25%) patients with solitary chest wall plasmacytoma (multiple myeloma), 1 of 6 (17%) patients with Ewing's sarcoma, and 2 of 4 (50%) of patients with osteogenic sarcoma. Although the five-year survival appears to indicate therapeutic success in patients with Ewing's sarcoma and osteogenic sarcoma, patients with chondrosarcoma or fibrosarcoma may have a more protracted course, and those with solitary plasmacytoma usually develop multiple myeloma. The findings suggest that radical surgical excision is the treatment of choice for chondrosarcoma; radical surgical excision combined with chemotherapy, for fibrosarcoma and osteogenic sarcoma; surgical excision combined with radiation and chemotherapy, for Ewing's sarcoma; and systemic surveillance and therapy, for pathologically confirmed solitary plasmacytoma.</description><identifier>ISSN: 0003-4975</identifier><identifier>EISSN: 1552-6259</identifier><identifier>DOI: 10.1016/S0003-4975(10)60906-X</identifier><identifier>PMID: 6959575</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Child ; Chondrosarcoma - therapy ; Female ; Fibrosarcoma - therapy ; Humans ; Male ; Middle Aged ; Multiple Myeloma - therapy ; Osteosarcoma - therapy ; Sarcoma, Ewing - therapy ; Thoracic Neoplasms - mortality ; Thoracic Neoplasms - therapy</subject><ispartof>The Annals of thoracic surgery, 1982-12, Vol.34 (6), p.664-673</ispartof><rights>1982 The Society of Thoracic Surgeons</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-95f4a0bd9c5eed68e3db530c77efd7402e1f823170f9c21319cb495bfc8cea683</citedby><cites>FETCH-LOGICAL-c442t-95f4a0bd9c5eed68e3db530c77efd7402e1f823170f9c21319cb495bfc8cea683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6959575$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Graeber, Geoffrey M.</creatorcontrib><creatorcontrib>Snyder, Robert J.</creatorcontrib><creatorcontrib>Fleming, Arthur W.</creatorcontrib><creatorcontrib>Head, Harold D.</creatorcontrib><creatorcontrib>Lough, Frederick C.</creatorcontrib><creatorcontrib>Parker, John S.</creatorcontrib><creatorcontrib>Zajtchuk, Rostik</creatorcontrib><creatorcontrib>Brott, Walter H.</creatorcontrib><title>Initial and Long-term Results in the Management of Primary Chest Wall Neoplasms</title><title>The Annals of thoracic surgery</title><addtitle>Ann Thorac Surg</addtitle><description>One hundred ten patients with primary chest wall neoplasms were analyzed for long-term results. The diagnosis of 59 malignant and 51 benign tumors was confirmed by the Armed Forces Institute of Pathology. No deaths were associated with primary definitive therapy. Among the five most frequently encountered malignant tumor types, five-year survivals were obtained in 9 of 17 (53%) patients with fibrosarcoma, 8 of 9 (89%) patients with chondrosarcoma, 2 of 8 (25%) patients with solitary chest wall plasmacytoma (multiple myeloma), 1 of 6 (17%) patients with Ewing's sarcoma, and 2 of 4 (50%) of patients with osteogenic sarcoma. Although the five-year survival appears to indicate therapeutic success in patients with Ewing's sarcoma and osteogenic sarcoma, patients with chondrosarcoma or fibrosarcoma may have a more protracted course, and those with solitary plasmacytoma usually develop multiple myeloma. The findings suggest that radical surgical excision is the treatment of choice for chondrosarcoma; radical surgical excision combined with chemotherapy, for fibrosarcoma and osteogenic sarcoma; surgical excision combined with radiation and chemotherapy, for Ewing's sarcoma; and systemic surveillance and therapy, for pathologically confirmed solitary plasmacytoma.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Child</subject><subject>Chondrosarcoma - therapy</subject><subject>Female</subject><subject>Fibrosarcoma - therapy</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multiple Myeloma - therapy</subject><subject>Osteosarcoma - therapy</subject><subject>Sarcoma, Ewing - therapy</subject><subject>Thoracic Neoplasms - mortality</subject><subject>Thoracic Neoplasms - therapy</subject><issn>0003-4975</issn><issn>1552-6259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EKqXwCZW8QrAI2E6cxCuEKh6VCkU8RHeW40xaI8cpcYLE35M2VbesRjP3zusgNKbkihIaX78RQsIgEgm_oOQyJoLEweIADSnnLIgZF4douLccoxPvv7qUdfIADWLBBU_4EM2nzjRGWaxcjmeVWwYN1CV-Bd_axmPjcLMC_KScWkIJrsFVgV9qU6r6F09W4Bv8qazFz1CtrfKlP0VHhbIeznZxhD7u794nj8Fs_jCd3M4CHUWsCQQvIkWyXGgOkMcphHnGQ6KTBIo8iQgDWqQspAkphGY0pEJnkeBZoVMNKk7DETrv567r6rvt7pCl8RqsVQ6q1su0-5SxKO6MvDfquvK-hkKu-_MlJXIDUm5Byg2lTWkLUi66vvFuQZuVkO-7duQ6_abXofvyx0AtvTbgNOSmBt3IvDL_bPgD3nyC0w</recordid><startdate>198212</startdate><enddate>198212</enddate><creator>Graeber, Geoffrey M.</creator><creator>Snyder, Robert J.</creator><creator>Fleming, Arthur W.</creator><creator>Head, Harold D.</creator><creator>Lough, Frederick C.</creator><creator>Parker, John S.</creator><creator>Zajtchuk, Rostik</creator><creator>Brott, Walter H.</creator><general>Elsevier Inc</general><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>198212</creationdate><title>Initial and Long-term Results in the Management of Primary Chest Wall Neoplasms</title><author>Graeber, Geoffrey M. ; Snyder, Robert J. ; Fleming, Arthur W. ; Head, Harold D. ; Lough, Frederick C. ; Parker, John S. ; Zajtchuk, Rostik ; Brott, Walter H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-95f4a0bd9c5eed68e3db530c77efd7402e1f823170f9c21319cb495bfc8cea683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Child</topic><topic>Chondrosarcoma - therapy</topic><topic>Female</topic><topic>Fibrosarcoma - therapy</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multiple Myeloma - therapy</topic><topic>Osteosarcoma - therapy</topic><topic>Sarcoma, Ewing - therapy</topic><topic>Thoracic Neoplasms - mortality</topic><topic>Thoracic Neoplasms - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Graeber, Geoffrey M.</creatorcontrib><creatorcontrib>Snyder, Robert J.</creatorcontrib><creatorcontrib>Fleming, Arthur W.</creatorcontrib><creatorcontrib>Head, Harold D.</creatorcontrib><creatorcontrib>Lough, Frederick C.</creatorcontrib><creatorcontrib>Parker, John S.</creatorcontrib><creatorcontrib>Zajtchuk, Rostik</creatorcontrib><creatorcontrib>Brott, Walter H.</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>The Annals of thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Graeber, Geoffrey M.</au><au>Snyder, Robert J.</au><au>Fleming, Arthur W.</au><au>Head, Harold D.</au><au>Lough, Frederick C.</au><au>Parker, John S.</au><au>Zajtchuk, Rostik</au><au>Brott, Walter H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Initial and Long-term Results in the Management of Primary Chest Wall Neoplasms</atitle><jtitle>The Annals of thoracic surgery</jtitle><addtitle>Ann Thorac Surg</addtitle><date>1982-12</date><risdate>1982</risdate><volume>34</volume><issue>6</issue><spage>664</spage><epage>673</epage><pages>664-673</pages><issn>0003-4975</issn><eissn>1552-6259</eissn><abstract>One hundred ten patients with primary chest wall neoplasms were analyzed for long-term results. The diagnosis of 59 malignant and 51 benign tumors was confirmed by the Armed Forces Institute of Pathology. No deaths were associated with primary definitive therapy. Among the five most frequently encountered malignant tumor types, five-year survivals were obtained in 9 of 17 (53%) patients with fibrosarcoma, 8 of 9 (89%) patients with chondrosarcoma, 2 of 8 (25%) patients with solitary chest wall plasmacytoma (multiple myeloma), 1 of 6 (17%) patients with Ewing's sarcoma, and 2 of 4 (50%) of patients with osteogenic sarcoma. Although the five-year survival appears to indicate therapeutic success in patients with Ewing's sarcoma and osteogenic sarcoma, patients with chondrosarcoma or fibrosarcoma may have a more protracted course, and those with solitary plasmacytoma usually develop multiple myeloma. The findings suggest that radical surgical excision is the treatment of choice for chondrosarcoma; radical surgical excision combined with chemotherapy, for fibrosarcoma and osteogenic sarcoma; surgical excision combined with radiation and chemotherapy, for Ewing's sarcoma; and systemic surveillance and therapy, for pathologically confirmed solitary plasmacytoma.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>6959575</pmid><doi>10.1016/S0003-4975(10)60906-X</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adolescent Adult Aged Child Chondrosarcoma - therapy Female Fibrosarcoma - therapy Humans Male Middle Aged Multiple Myeloma - therapy Osteosarcoma - therapy Sarcoma, Ewing - therapy Thoracic Neoplasms - mortality Thoracic Neoplasms - therapy |
title | Initial and Long-term Results in the Management of Primary Chest Wall Neoplasms |
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