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dc.contributor.authorKiter G.
dc.contributor.authorMüsellim B.
dc.contributor.authorÇetinkaya E.
dc.contributor.authorTürker H.
dc.contributor.authorKunt Uzaslan A.E.
dc.contributor.authorYentürk E.
dc.contributor.authorÖngen G.
dc.date.accessioned2020-06-21T09:37:18Z
dc.date.available2020-06-21T09:37:18Z
dc.date.issued2011
dc.identifier.issn0494-1373
dc.identifier.urihttps://doi.org/10.5578/tt.2495
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4716
dc.descriptionPubMed: 22087521en_US
dc.description.abstractSarcoidosis is an idiopathic granulomatous disease. It usually affects the lung. The diagnosis may be problematic since the known causes of granulomatous inflammation must be excluded. This multicenter study aimed to evaluate the clinical presentations and diagnostic approaches of sarcoidosis. The study protocol was sent via internet, and the participants were asked to send the information (clinical, radiological and diagnostic) on newly diagnosed sarcoidosis cases. 293 patients were enrolled within two years. Pulmonary symptoms were found in 73.3% of the patients, and cough was the most common one (53.2%), followed by dyspnea (40.3%). Constitutional symptoms were occured in half of the patients. The most common one was fatigue (38.6%). The most common physical sign was eritema nodosum (17.1%). The most common chest radiograhical sign was bilateral hilar lymphadenomegaly (78.8%). Staging according to chest X-ray has revealed that most of the patients were in Stage I and Stage II (51.9% and 31.7%, respectively). Sarcoidosis was confirmed histopathologically in 265 (90.4%) patients. Although one-third of the bronchoscopy was revealed normal, mucosal hyperemi (19.8%) and external compression of the bronchial wall (16.8%) were common abnormal findings. The 100% success rate was obtained in mediastinoscopy among the frequently used sampling methods. Transbronchial biopsy was the most frequently used method with 48.8% success rate. Considering sarcoidosis with its most common and also rare findings in the differential diagnosis, organizing the related procedures according to the possibly effected areas, and the expertise of the team would favor multimodality diagnosis.en_US
dc.language.isoengen_US
dc.publisherAnkara Universityen_US
dc.relation.isversionof10.5578/tt.2495en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDiagnosisen_US
dc.subjectPulmonaryen_US
dc.subjectSarcoidosisen_US
dc.titleClinical presentations and diagnostic work-up in sarcoidosis: A series of Turkish cases (clinics and diagnosis of sarcoidosis)en_US
dc.title.alternativeSarkoidozlu olgularda klinik görünüm ve tanısal yaklaşım: Türk olgu serisi (sarkoidoz kliniği ve tanı yaklaşımları)en_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume59en_US
dc.identifier.issue3en_US
dc.identifier.startpage248en_US
dc.identifier.endpage258en_US
dc.relation.journalTuberkuloz ve Toraksen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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