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dc.contributor.authorGürel, Gülhan
dc.contributor.authorÖzdemir, Çiğdem
dc.contributor.authorDurusu, İrem Nur
dc.date.accessioned2022-05-17T06:32:10Z
dc.date.available2022-05-17T06:32:10Z
dc.date.issued07.04.2022en_US
dc.identifier.citationGürel, G., Özdemir, Ç., & Durusu, İ. N. (2022). Cutaneous tuberculosis induced by adalimumab. Dermatologic Therapy, e15503-e15503.en_US
dc.identifier.issn1529-8019
dc.identifier.urihttps://doi.org/10.1111/dth.15503
dc.identifier.urihttps://hdl.handle.net/20.500.12933/1022
dc.description.abstractDear Editor, Adalimumab (Humira®, AbbVie Inc., North Chicago, IL, USA) is a fully human monoclonal antibody specific for tumor necrosis factor-α (TNF-α) that is approved for the treatment of moderate-to-severe hidradenitis suppurativa who did not respond to classical systemic treatment.1 Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease that is characterized by recurrent painful nodules, abscesses and draining sinus tracts mainly in intertriginous areas. It could cause severe impact on patients' quality of life.2 Patients treated with TNF-α antagonists are at increased risk for tuberculosis during treatment. And if that occurs they usually present with disseminated or extrapulmonary disease.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1111/dth.15503en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.titleCutaneous tuberculosis induced by adalimumaben_US
dc.typearticleen_US
dc.authorid0000-0001-5716-8750en_US
dc.authorid0000-0001-8500-0744en_US
dc.authorid0000-0003-2072-3268en_US
dc.departmentAFSÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Deri ve Zührevi Hastalıklar Ana Bilim Dalıen_US
dc.contributor.institutionauthorGürel, Gülhan
dc.contributor.institutionauthorÖzdemir, Çiğdem
dc.contributor.institutionauthorDurusu, İrem Nur
dc.identifier.startpage1en_US
dc.identifier.endpage3en_US
dc.relation.journalDermatologic Therapyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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