Fibrosarcoma in Children: A Rare Tumour with Long-Term Survival even with Advanced Disease A Report of 3 Cases
Fibrosarcoma is a rare tumour in children. The potential of malignancy has been questioned. We present three cases of fibrosarcoma in children. The follow-up periods range from 10 to 37 years. The first patient had pulmonary metastases at the time of diagnosis in 1958. The primary tumour in fossa is...
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| Veröffentlicht in: | Acta oncologica 1997, Vol.36 (4), p.438-440 |
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| container_title | Acta oncologica |
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| creator | Lilleng, Peer K. Monge, Odd R. Walløe, Anders Trovik, Clement S. Hordvik, Markus Høie, Johan Dahl, Olav Bang, Gisle |
| description | Fibrosarcoma is a rare tumour in children. The potential of malignancy has been questioned. We present three cases of fibrosarcoma in children. The follow-up periods range from 10 to 37 years. The first patient had pulmonary metastases at the time of diagnosis in 1958. The primary tumour in fossa ischio-rectalis was resected in 1960. Lung metastases were resected in 1960 and 1989. Radiotherapy was given in 1992. He is still alive with metastases 37 years after the first manifestation of disease. The second patient had a primary tumour and several local recurrences in the mandible. He is alive without evidence of disease 4 years after resection of pulmonary metastases and 21 years after resection of the primary tumour. The third patient has no signs of recurrence or metastasic spread 10 years after a wide excision of subcutanous tumours of the left upper arm. The cases demonstrate a special tumour-entity of low-grade malignancy, which show a good prognosis and a wide spectrum of biological behaviour. |
| doi_str_mv | 10.3109/02841869709001294 |
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The potential of malignancy has been questioned. We present three cases of fibrosarcoma in children. The follow-up periods range from 10 to 37 years. The first patient had pulmonary metastases at the time of diagnosis in 1958. The primary tumour in fossa ischio-rectalis was resected in 1960. Lung metastases were resected in 1960 and 1989. Radiotherapy was given in 1992. He is still alive with metastases 37 years after the first manifestation of disease. The second patient had a primary tumour and several local recurrences in the mandible. He is alive without evidence of disease 4 years after resection of pulmonary metastases and 21 years after resection of the primary tumour. The third patient has no signs of recurrence or metastasic spread 10 years after a wide excision of subcutanous tumours of the left upper arm. The cases demonstrate a special tumour-entity of low-grade malignancy, which show a good prognosis and a wide spectrum of biological behaviour.</description><identifier>ISSN: 0284-186X</identifier><identifier>EISSN: 1651-226X</identifier><identifier>DOI: 10.3109/02841869709001294</identifier><identifier>PMID: 9247108</identifier><identifier>CODEN: ACTOEL</identifier><language>eng</language><publisher>Basingstoke: Informa UK Ltd</publisher><subject>Abdominal Neoplasms - pathology ; Abdominal Neoplasms - surgery ; Adolescent ; Biological and medical sciences ; Child, Preschool ; Disease-Free Survival ; Fibrosarcoma - pathology ; Fibrosarcoma - secondary ; Fibrosarcoma - surgery ; Follow-Up Studies ; Humans ; Infant ; Lung Neoplasms - secondary ; Lung Neoplasms - surgery ; Male ; Mandibular Neoplasms - pathology ; Mediastinal Neoplasms - secondary ; Medical sciences ; Mitosis ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Muscle Neoplasms - pathology ; Neoplasm Recurrence, Local - pathology ; Survival Rate ; Tumors ; Vimentin - analysis</subject><ispartof>Acta oncologica, 1997, Vol.36 (4), p.438-440</ispartof><rights>1997 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-1727e46e03202016625c38e3a3f9cd1e43d82a70de99fd56d64bc67d7707790f3</citedby><cites>FETCH-LOGICAL-c352t-1727e46e03202016625c38e3a3f9cd1e43d82a70de99fd56d64bc67d7707790f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/02841869709001294$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/02841869709001294$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,780,784,4024,27923,27924,27925,61221,61402</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2736635$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9247108$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lilleng, Peer K.</creatorcontrib><creatorcontrib>Monge, Odd R.</creatorcontrib><creatorcontrib>Walløe, Anders</creatorcontrib><creatorcontrib>Trovik, Clement S.</creatorcontrib><creatorcontrib>Hordvik, Markus</creatorcontrib><creatorcontrib>Høie, Johan</creatorcontrib><creatorcontrib>Dahl, Olav</creatorcontrib><creatorcontrib>Bang, Gisle</creatorcontrib><title>Fibrosarcoma in Children: A Rare Tumour with Long-Term Survival even with Advanced Disease A Report of 3 Cases</title><title>Acta oncologica</title><addtitle>Acta Oncol</addtitle><description>Fibrosarcoma is a rare tumour in children. The potential of malignancy has been questioned. We present three cases of fibrosarcoma in children. The follow-up periods range from 10 to 37 years. The first patient had pulmonary metastases at the time of diagnosis in 1958. The primary tumour in fossa ischio-rectalis was resected in 1960. Lung metastases were resected in 1960 and 1989. Radiotherapy was given in 1992. He is still alive with metastases 37 years after the first manifestation of disease. The second patient had a primary tumour and several local recurrences in the mandible. He is alive without evidence of disease 4 years after resection of pulmonary metastases and 21 years after resection of the primary tumour. The third patient has no signs of recurrence or metastasic spread 10 years after a wide excision of subcutanous tumours of the left upper arm. The cases demonstrate a special tumour-entity of low-grade malignancy, which show a good prognosis and a wide spectrum of biological behaviour.</description><subject>Abdominal Neoplasms - pathology</subject><subject>Abdominal Neoplasms - surgery</subject><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child, Preschool</subject><subject>Disease-Free Survival</subject><subject>Fibrosarcoma - pathology</subject><subject>Fibrosarcoma - secondary</subject><subject>Fibrosarcoma - surgery</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Lung Neoplasms - secondary</subject><subject>Lung Neoplasms - surgery</subject><subject>Male</subject><subject>Mandibular Neoplasms - pathology</subject><subject>Mediastinal Neoplasms - secondary</subject><subject>Medical sciences</subject><subject>Mitosis</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Muscle Neoplasms - pathology</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Survival Rate</subject><subject>Tumors</subject><subject>Vimentin - analysis</subject><issn>0284-186X</issn><issn>1651-226X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEGLEzEUx4Moa3f1A3gQcpC9jfuSzCQTPZW6qwsFQSvsbUiTNzbLTFKTmYrf3pSWvQieHuT_e_8XfoS8YfBeMNA3wNuatVIr0ACM6_oZWTDZsIpz-fCcLI55VYCHl-Qy50cA4EI1F-RC81oxaBck3PltitkkG0dDfaCrnR9cwvCBLuk3k5Bu5jHOif72046uY_hZbTCN9PucDv5gBooHDKdw6Q4mWHT0k89oMh4LcB_TRGNPBV2Vp_yKvOjNkPH1eV6RH3e3m9WXav318_1qua6saPhUMcUV1hJBcODApOSNFS0KI3ptHcNauJYbBQ617l0jnay3ViqnFCiloRdX5PrUu0_x14x56kafLQ6DCRjn3CldTjTACshOoC0WcsK-2yc_mvSnY9AdHXf_OC47b8_l83ZE97Rxllryd-fcZGuGPhUtPj9hXAkpRVOwjyfMhz6m0ezQDNPOFufdYzEeip__fOIvfuqUTA</recordid><startdate>1997</startdate><enddate>1997</enddate><creator>Lilleng, Peer K.</creator><creator>Monge, Odd R.</creator><creator>Walløe, Anders</creator><creator>Trovik, Clement S.</creator><creator>Hordvik, Markus</creator><creator>Høie, Johan</creator><creator>Dahl, Olav</creator><creator>Bang, Gisle</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>IQODW</scope><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>1997</creationdate><title>Fibrosarcoma in Children: A Rare Tumour with Long-Term Survival even with Advanced Disease A Report of 3 Cases</title><author>Lilleng, Peer K. ; Monge, Odd R. ; Walløe, Anders ; Trovik, Clement S. ; Hordvik, Markus ; Høie, Johan ; Dahl, Olav ; Bang, Gisle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-1727e46e03202016625c38e3a3f9cd1e43d82a70de99fd56d64bc67d7707790f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Abdominal Neoplasms - pathology</topic><topic>Abdominal Neoplasms - surgery</topic><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child, Preschool</topic><topic>Disease-Free Survival</topic><topic>Fibrosarcoma - pathology</topic><topic>Fibrosarcoma - secondary</topic><topic>Fibrosarcoma - surgery</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Lung Neoplasms - secondary</topic><topic>Lung Neoplasms - surgery</topic><topic>Male</topic><topic>Mandibular Neoplasms - pathology</topic><topic>Mediastinal Neoplasms - secondary</topic><topic>Medical sciences</topic><topic>Mitosis</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Muscle Neoplasms - pathology</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Survival Rate</topic><topic>Tumors</topic><topic>Vimentin - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lilleng, Peer K.</creatorcontrib><creatorcontrib>Monge, Odd R.</creatorcontrib><creatorcontrib>Walløe, Anders</creatorcontrib><creatorcontrib>Trovik, Clement S.</creatorcontrib><creatorcontrib>Hordvik, Markus</creatorcontrib><creatorcontrib>Høie, Johan</creatorcontrib><creatorcontrib>Dahl, Olav</creatorcontrib><creatorcontrib>Bang, Gisle</creatorcontrib><collection>Pascal-Francis</collection><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>Acta oncologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lilleng, Peer K.</au><au>Monge, Odd R.</au><au>Walløe, Anders</au><au>Trovik, Clement S.</au><au>Hordvik, Markus</au><au>Høie, Johan</au><au>Dahl, Olav</au><au>Bang, Gisle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fibrosarcoma in Children: A Rare Tumour with Long-Term Survival even with Advanced Disease A Report of 3 Cases</atitle><jtitle>Acta oncologica</jtitle><addtitle>Acta Oncol</addtitle><date>1997</date><risdate>1997</risdate><volume>36</volume><issue>4</issue><spage>438</spage><epage>440</epage><pages>438-440</pages><issn>0284-186X</issn><eissn>1651-226X</eissn><coden>ACTOEL</coden><abstract>Fibrosarcoma is a rare tumour in children. The potential of malignancy has been questioned. We present three cases of fibrosarcoma in children. The follow-up periods range from 10 to 37 years. The first patient had pulmonary metastases at the time of diagnosis in 1958. The primary tumour in fossa ischio-rectalis was resected in 1960. Lung metastases were resected in 1960 and 1989. Radiotherapy was given in 1992. He is still alive with metastases 37 years after the first manifestation of disease. The second patient had a primary tumour and several local recurrences in the mandible. He is alive without evidence of disease 4 years after resection of pulmonary metastases and 21 years after resection of the primary tumour. The third patient has no signs of recurrence or metastasic spread 10 years after a wide excision of subcutanous tumours of the left upper arm. 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| source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Taylor & Francis Journals Complete |
| subjects | Abdominal Neoplasms - pathology Abdominal Neoplasms - surgery Adolescent Biological and medical sciences Child, Preschool Disease-Free Survival Fibrosarcoma - pathology Fibrosarcoma - secondary Fibrosarcoma - surgery Follow-Up Studies Humans Infant Lung Neoplasms - secondary Lung Neoplasms - surgery Male Mandibular Neoplasms - pathology Mediastinal Neoplasms - secondary Medical sciences Mitosis Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Muscle Neoplasms - pathology Neoplasm Recurrence, Local - pathology Survival Rate Tumors Vimentin - analysis |
| title | Fibrosarcoma in Children: A Rare Tumour with Long-Term Survival even with Advanced Disease A Report of 3 Cases |
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