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Intrathoracic malignant peripheral nerve sheath tumor with angiosarcoma in a child with NF1

dc.contributor.authorElli M.
dc.contributor.authorCan B.
dc.contributor.authorCeyhan M.
dc.contributor.authorPinarli F.G.
dc.contributor.authorDağdemir A.
dc.contributor.authorAyyildiz H.S.
dc.contributor.authorDağçinar A.
dc.date.accessioned2020-06-21T09:25:03Z
dc.date.available2020-06-21T09:25:03Z
dc.date.issued2007
dc.identifier.issn0300-8916
dc.identifier.urihttps://doi.org/10.1177/030089160709300625
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3917
dc.descriptionPubMed: 18338507en_US
dc.description.abstractMalignant peripheral nerve sheath tumors (MPNSTs) are uncommon in children and adolescents but occur more frequently in NF1 patients. Angiosarcomatous differentiation in MPNSTs is a rare entity with poor prognosis. We report on a 13-year-old boy with intrathoracic angiosarcoma arising in MPNST associated with NF1.en_US
dc.language.isoengen_US
dc.publisherIl Pensiero Scientifico Editore s.r.l.en_US
dc.relation.isversionof10.1177/030089160709300625en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAngiosarcomaen_US
dc.subjectChildhooden_US
dc.subjectMalignant peripheral nerve sheath tumorsen_US
dc.subjectNF1en_US
dc.titleIntrathoracic malignant peripheral nerve sheath tumor with angiosarcoma in a child with NF1en_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume93en_US
dc.identifier.issue6en_US
dc.identifier.startpage641en_US
dc.identifier.endpage644en_US
dc.relation.journalTumorien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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