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Pulmonary langerhans cell histiocytosis [Pulmoner langerhans hücreli histiyositoz]

dc.contributor.authorÇelik B.
dc.contributor.authorFurtun K.
dc.contributor.authorBilgin S.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:31:14Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:31:14Z
dc.date.issued2010
dc.identifier.issn1302-7808
dc.identifier.urihttps://dx.doi.org/10.5152/ttd.2010.08
dc.identifier.urihttps://hdl.handle.net/20.500.12418/5131
dc.description.abstractPulmonary Langerhans cell histiocytosis is an uncommon interstitial lung disease that results from the accumulation of cells known as Langerhans cells in the lung. It primarily affects young smokers. High resolution chest computed tomography findings are typical for the disease. Open lung biopsy is an effective method in the diagnosis of the disease. In the present report we describe two patients with pulmonary Langerhans cell histiocytosis diagnosed by open lung biopsy.en_US
dc.description.sponsorshipÇelik, B.; 19 Mayis Üniversitesi Tip Fakültesi, Gö?üs Cerrahisi Anabilim Dali, Samsun, Turkey; email: cburcin@hotmail.comen_US
dc.language.isoturen_US
dc.relation.isversionof10.5152/ttd.2010.08en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectLangerhans cell histiocytosisen_US
dc.subjectOpen lung biopsyen_US
dc.subjectPneumothoraxen_US
dc.titlePulmonary langerhans cell histiocytosis [Pulmoner langerhans hücreli histiyositoz]en_US
dc.typearticleen_US
dc.relation.journalTurk Toraks Dergisien_US
dc.contributor.departmentÇelik, B., Cumhuriyet Üniversitesi Tip Fakültesi, Gö?üs Cerrahisi Anabilim Dali, Sivas, Turkey -- Furtun, K., Samsun Gö?üs Hastaliklari ve Gö?üs Cerrahisi Hastanesi, Samsun, Turkey -- Bilgin, S., Samsun Gö?üs Hastaliklari ve Gö?üs Cerrahisi Hastanesi, Samsun, Turkeyen_US
dc.identifier.volume11en_US
dc.identifier.issue2en_US
dc.identifier.endpage86en_US
dc.identifier.startpage84en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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