Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/28921
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dc.date.accessioned2022-10-03T07:25:13Z-
dc.date.available2022-10-03T07:25:13Z-
dc.date.issued2012-12-
dc.identifier.citationTuran, A. vd. (2012). "IVIG tedavisine yanıt veren bir monoklonal gamopatisiz skleromiksödem olgusu". Turkderm-Turkish Archives of Dermatology and Venerology, 46(4), 223-225.tr_TR
dc.identifier.issn2717-6398-
dc.identifier.issn2651-5164-
dc.identifier.urihttps://doi.org/10.4274/Turkderm.29291-
dc.identifier.urihttps://journal.turkderm.org.tr/eng/jvi.aspx?pdir=turkderm&plng=eng&un=TURKDERM-29291-
dc.identifier.urihttp://hdl.handle.net/11452/28921-
dc.description.abstract‘‘Liken miksödematozus’’ deride fibroblast artışı ve müsin birikimi ile karakterize primer inflamatuvar bir dermatozdur. Skleromiksödem liken miksödematozusun jeneralize formu olup papüler lezyonlar, difüz skleroz ve eritem ile seyreder. Sıklıkla paraproteinemilerle birliktelik gösterir. Monoklonal gamopatisiz skleromiksödem ise liken miksödematozusun daha nadir görülen atipik bir varyantıdır. Sistemik tutulum da gösterebilen ve bazen fatal olabilen hastalığın tedavisinde olgu bildirileri şeklinde çok çeşitli seçenekler denense de henüz kesin bir tedavi şekli yoktur. İntravenöz immünglobulin ile yapılan olgu bildirilerinde ise yüz güldürücü sonuçlar elde edilmiştir. Skleromiksödemin etyopatogenezi tam olarak anlaşılamadığı gibi intravenöz immünglobulinin de skleromiksödemdeki etki mekanizması hâlen net değildir. Burada monoklonal gamopatinin eşlik etmediği bir skleromiksödem olgusu ve intravenöz immünglobulin tedavisine yanıtı sunulmaktadır.tr_TR
dc.description.abstractLichen myxedematosus is a primary inflammatory dermatosis characterized by fibroblast proliferation and mucin deposition in the skin. Scleromyxedema is the generalized variant of lichen myxedematosus and is accompanied by papular lesions, diffuse sclerosis and erythema. It is usually associated with paraproteinemias. Scleromyxedema without monoclonal gammopathy is a rare and atypical variant of lichen myxedematosus. Systemic involvement and sometimes fatal course can be seen with scleromyxedema. Although several treatment modalities have been tried, there is no definitive treatment available for the disease. Satisfactory results have been obtained in the case reports in which intravenous immunoglobulin treatment was used.The mechanism of action of intravenous immunoglobulin in scleromyxedema is still not clear as well as the etiopathogenesis of scleromyxedema. Herein, we describe the case of a patient with scleromyxedema without monoclonal gammopathy and his response to the treatment with intravenous immunoglobulin.en_US
dc.language.isotrtr_TR
dc.publisherDeri Zührevi Hastalıklar Derneğitr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectDermatologyen_US
dc.subjectIVIGen_US
dc.subjectMonoclonal gammopathyen_US
dc.subjectScleromyxedemaen_US
dc.subjectTreatmenten_US
dc.subjectLichen myxedematosusen_US
dc.subjectPapular mucinosisen_US
dc.subjectMonoklonal gamopatien_US
dc.subjectSkleromiksödemen_US
dc.subjectTedavitr_TR
dc.titleIVIG tedavisine yanıt veren bir monoklonal gamopatisiz skleromiksödem olgusutr_TR
dc.title.alternativeA case of scleromyxedema without monoclonal gammopathy responded to treatment with IVIGen_US
dc.typeArticleen_US
dc.identifier.wos000313861400013tr_TR
dc.identifier.scopus2-s2.0-84873659956tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludaǧ Üniversitesi/Tıp Fakültesi/Deri ve Zührevi Hastalıklar Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-0193-1128tr_TR
dc.contributor.orcid0000-0002-5039-164Xtr_TR
dc.contributor.orcid0000-0003-3801-2835tr_TR
dc.identifier.startpage223tr_TR
dc.identifier.endpage225tr_TR
dc.identifier.volume46tr_TR
dc.identifier.issue4tr_TR
dc.relation.journalTurkderm-Turkish Archives of Dermatology and Venerologyen_US
dc.contributor.buuauthorTuran, Ayşegül-
dc.contributor.buuauthorAydoğan, Kenan-
dc.contributor.buuauthorAdım, Şaduman Balaban-
dc.contributor.buuauthorSarıcaoğlu, Hayriye-
dc.contributor.researcheridEAG-5053-2022tr_TR
dc.contributor.researcheridENI-5150-2022tr_TR
dc.contributor.researcheridEMN-0789-2022tr_TR
dc.contributor.researcheridDPU-8534-2022tr_TR
dc.relation.collaborationYurt içitr_TR
dc.indexed.trdizinTrDizintr_TR
dc.subject.wosDermatologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.contributor.scopusid14055302400tr_TR
dc.contributor.scopusid9739755800tr_TR
dc.contributor.scopusid15730076300tr_TR
dc.contributor.scopusid6603722836tr_TR
dc.subject.scopusScleromyxedema; Mucinoses; Paraproteinsen_US
dc.subject.emtreeImmunoglobulinen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMonoclonal immunoglobulinemiaen_US
dc.subject.emtreeScleromyxedemaen_US
dc.subject.emtreeTreatment responseen_US
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