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dc.contributor.authorSeyhan, Ekrem Cengiz
dc.contributor.authorSokucu, Sinem Nedime
dc.contributor.authorGünlüoğlu, Gülşah
dc.contributor.authorŞimşek Veske, Nurdan
dc.contributor.authorAltın, Sedat
dc.date.accessioned2020-07-01T14:57:24Z
dc.date.available2020-07-01T14:57:24Z
dc.date.issued2014en_US
dc.identifier.citationSeyhan, E. C., Sokucu, S. N., Günlüoğlu, G., Şimşek Veske, N. ve Altın, S. (2014). Primary pulmonary synovial sarcoma: A very rare presentation. Case Reports in Pulmonology, 2014. http://dx.doi.org/10.1155/2014/537618en_US
dc.identifier.issn2090-6846
dc.identifier.issn2090-6854
dc.identifier.urihttp://dx.doi.org/10.1155/2014/537618
dc.identifier.urihttps://hdl.handle.net/20.500.12511/5367
dc.description.abstractSynovial sarcoma (SS) is a rare tumor originating from mesenchymal tissue and accounting for approximately 5–10% of all soft tissue sarcomas. A rare case of primary pulmonary SS in an asymptomatic 18-year-old man admitted to our hospital for investigation of a 6 × 6.5 cm, oval-shaped, well-delineated pleural based peripheral mass in the left lower lobe in his thorax CT is presented. Left lower lobectomy was done. Immunohistochemically, tumor cells were positive for cytokeratin, epithelial membrane antigen (EMA), and vimentin so that the histopathological diagnosis was compatible with biphasic spindle cell type SS in the lung.en_US
dc.language.isoengen_US
dc.publisherHindawi Publishing Corporationen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPrimary Pulmonary Synovial Sarcomaen_US
dc.subjectPresentationen_US
dc.subjectChest Diseasesen_US
dc.titlePrimary pulmonary synovial sarcoma: A very rare presentationen_US
dc.typearticleen_US
dc.relation.journalCase Reports in Pulmonologyen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Göğüs Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0001-6639-2797en_US
dc.identifier.volume2014en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1155/2014/537618en_US


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