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Clinical outcome of parosteal osteosarcoma

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dc.contributor.authorHan, Ilkyu-
dc.contributor.authorOh, Joo Han-
dc.contributor.authorNa, Yeong Gon-
dc.contributor.authorMoon, Kyung Chul-
dc.contributor.authorKim, Han-Soo-
dc.date.accessioned2010-04-30T05:09:03Z-
dc.date.available2010-04-30T05:09:03Z-
dc.date.issued2007-12-01-
dc.identifier.citationJ Surg Oncol. 2008 ;97(2):146-9.en
dc.identifier.issn0022-4790 (Print)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=18050289-
dc.identifier.urihttps://hdl.handle.net/10371/63581-
dc.description.abstractBACKGROUND: Parosteal osteosarcoma is a rare type of osteosarcoma with distinct characteristics. Clinical outcome of 21 patients was analyzed to assess the predictive relevance of surgical margin, intramedullary tumor extension and histologic grade. METHODS: There were 5 mens and 16 womens with an average age of 26 years. Average follow-up was 9.1 years (range 2.5-22.1). Most common sites were distal femur (15) and proximal humerus (2). No patient presented with metastasis. Surgical margin was wide in 13 and marginal in 8. Intramedullary extension was seen in 10 patients (48%). Focal high-grade 2 and 3 tumors were seen in 11 (52%) and 3 (14%) patients respectively. RESULTS: Twenty patients (95%) were alive without disease. Two (10%) had relapse, one with local recurrence and another with local recurrence and lung metastasis. Of eight marginal procedures performed, 2 turned out to have histologically tumor-positive margins, both of whom later developed relapses. All patients with histologically negative margins remained disease-free. Presence of intramedullary extension and focal high-grade tumor was not significantly associated with relapse. CONCLUSIONS: A marginal but histologically negative margin of excision appears adequate for parosteal osteosarcoma. However, long-term follow-up is warranted for monitoring of rare incidences of local recurrences or distant metastases.en
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectBone Marrow/surgeryen
dc.subjectBone Neoplasms/*surgeryen
dc.subjectDisease-Free Survivalen
dc.subjectFemaleen
dc.subjectFemoral Neoplasms/surgeryen
dc.subjectFibula/surgeryen
dc.subjectFollow-Up Studiesen
dc.subjectHumansen
dc.subjectHumerus/surgeryen
dc.subjectIlium/surgeryen
dc.subjectLung Neoplasms/secondaryen
dc.subjectMaleen
dc.subjectNeoplasm Invasivenessen
dc.subjectNeoplasm Recurrence, Local/pathologyen
dc.subjectNeoplasm, Residualen
dc.subjectOsteosarcoma, Juxtacortical/secondary/*surgeryen
dc.subjectRetrospective Studiesen
dc.subjectTibia/surgeryen
dc.subjectTreatment Outcomeen
dc.titleClinical outcome of parosteal osteosarcomaen
dc.typeArticleen
dc.contributor.AlternativeAuthor한일규-
dc.contributor.AlternativeAuthor오주한-
dc.contributor.AlternativeAuthor나영곤-
dc.contributor.AlternativeAuthor문경철-
dc.contributor.AlternativeAuthor김한수-
dc.identifier.doi10.1002/jso.20902-
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