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Dedifferentiated solitary fibrous tumor of thoracic cavity

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dc.contributor.authorYang, J.W.-
dc.contributor.authorSong, D.H.-
dc.contributor.authorJang, I.S.-
dc.contributor.authorKo, G.H.-
dc.date.accessioned2022-12-27T00:04:39Z-
dc.date.available2022-12-27T00:04:39Z-
dc.date.issued2014-
dc.identifier.issn1738-1843-
dc.identifier.issn2092-8920-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/20133-
dc.description.abstractSolitary fibrous tumor (SFT) is a mesenchymal tumor characterized by fibroblast-like tumor cells, thick collagen bands, a hemangiopericytoma-like branching vascular pattern and CD34 expression of tumor cells.1 Although some cases show malignant behavior, most of the cases are benign and have histologically bland-looking tumor cells. Rarely, highly pleomorphic sarcoma arises within a primary or recurrent SFT having typical histologic features. This is a phenomenon similar to that seen in dedifferentiated liposarcoma. Dedifferentiated SFT (DSFT) is rare, with less than 30 cases reported worldwide,2-6 and it has not been previously reported in Korea. Here, we present a case of DSFT. ? 2014 The Korean Society of Pathologists.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherSeoul National University-
dc.titleDedifferentiated solitary fibrous tumor of thoracic cavity-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4132/KoreanJPathol.2014.48.3.250-
dc.identifier.scopusid2-s2.0-84903752554-
dc.identifier.bibliographicCitationKorean Journal of Pathology, v.48, no.3, pp 250 - 253-
dc.citation.titleKorean Journal of Pathology-
dc.citation.volume48-
dc.citation.number3-
dc.citation.startPage250-
dc.citation.endPage253-
dc.type.docTypeArticle-
dc.identifier.kciidART001884144-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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