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dc.contributor.authorMat, M. Cem
dc.date.accessioned2021-03-03T10:00:37Z
dc.date.available2021-03-03T10:00:37Z
dc.identifier.citationMat M. C. , "Treatment of Behcet's Disease", TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, cilt.43, ss.92-97, 2009
dc.identifier.issn1019-214X
dc.identifier.othervv_1032021
dc.identifier.otherav_201d2b89-c402-4726-b07f-8fa4cd322afe
dc.identifier.urihttp://hdl.handle.net/20.500.12627/26677
dc.identifier.urihttps://doi.org/10.1016/j.revmed.2009.09.023
dc.description.abstractBehcet disease is a chronic disease of unknown etiology. It is a systemic vasculitis which can affect many systems and the disease course may be severe in young males. The main aim of treatment is to reduce inflammation and control symptoms of the disease. The main principle of treatment is to prevent attacks of inflammation, reduce symptoms and prevent relapses. Antiinflammatory and immunomodulatory drugs are used for these aims. In this paper, double blinded placebo controlled studies, open studies and case reports have been reviewed to form an update of current treatments. Interferon alpha and TNF antagonists are preferred especially for severe eye involvement. TNF alpha inhibitors have been shown to be effective for neurologic involvement, one of the most severe complications of the disease. Besides these, the guidelines of the Behcet Disease Expert Commission of the European Rheumatism Association (EULAR) have been reviewed. A multidisciplinary approach is necessary to assess the patients' clinical and laboratory status and prevent side effects of treatment. (Turkderm 2009; 43 Suppl 2: 92-7)
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDermatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.titleTreatment of Behcet's Disease
dc.typeMakale
dc.relation.journalTURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY
dc.contributor.department, ,
dc.identifier.volume43
dc.identifier.startpage92
dc.identifier.endpage97
dc.contributor.firstauthorID194176


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