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dc.creatorConstanza Navarrete, María Alejandra López Arias, Mauricio Peláezspa
dc.creatorCarrillo Jorge Albertospa
dc.date.accessioned2018-07-02T03:23:59Z
dc.date.available2018-07-02T03:23:59Z
dc.date.created2014spa
dc.identifier.urihttp://repositorio.mederi.com.co/handle/123456789/129
dc.description.abstractAbstract: Primary pleural liposarcoma (PPL) is a rare tumor derived from primitive mesenchymal tissue. We report a case of a 49-year-old female patient complaining of thoracic pain and dyspnea for 3 months. The chest X-ray showed a left basal opacity of lobulated contours and the thoracic computer tomography (CT) scan revealed a left pleural collection/mass, of 18 HU density and passive pulmonary atelectasis. The patient was taken to surgery and the cytologic examination of the gelatinous mass found in the procedure confirmed the diagnosis of a pleomorphic variant of pleural liposarcoma. We emphasise in the importance of careful inspection of the origin of the tumor in the diagnostic images to allow accurate diagnosis. Keywords: Primary pleural liposarcoma (PPL); pleomorphic variant; thoracic computer tomography; pleural neoplasmsen
dc.format.mimetypeapplication/pdfspa
dc.languageengspa
dc.publisherJournal of Thoracic Diseasespa
dc.relation.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178095/pdf/jtd-06-09-E166.pdfspa
dc.titlePrimary pleural liposarcoma, pleomorphic variant.spa
dc.typeinfo:eu-repo/semantics/articlespa
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessspa
dc.type.spaartículospa
dc.rights.accesoAbierto (Texto completo)spa


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