Primary pulmonary synovial sarcoma: A very rare presentation

dc.authorid0000-0001-6639-2797
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.issued2014
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Göğüs Hastalıkları Ana Bilim Dalı
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.
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/10.1155/2014/537618
dc.identifier.doi10.1155/2014/537618
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.identifier.volume2014
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherHindawi Publishing Corporation
dc.relation.ispartofCase Reports in Pulmonologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPrimary Pulmonary Synovial Sarcoma
dc.subjectPresentation
dc.subjectChest Diseases
dc.titlePrimary pulmonary synovial sarcoma: A very rare presentation
dc.typeArticle

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