A case of angioedema-like atypic scleromyxedema responding to treatment with steroid

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dc.contributor.authorPolat, Aysegul
dc.contributor.authorKapicioglu, Yelda
dc.contributor.authorSahin, Nurhan
dc.contributor.authorYilmaz, Mikail
dc.date.accessioned2024-08-04T20:41:40Z
dc.date.available2024-08-04T20:41:40Z
dc.date.issued2016
dc.departmentİnönü Üniversitesien_US
dc.description.abstractLichen myxedematosus is a chronic, inflammatory, systemic dermatose characterized by dermal musin deposition and increased fibroblasts in the absence of thyroid dysfunction. It is usually seen together with paraproteinemia. It is clinically classified as scleromyxedema (papular mucinosis), localized lichen myxedematosus, and atypical lichen myxedematosus. Etiopathogenesis of the disease which is very difficult to treat is still unknown. Herein, we present a case of atypical scleromyxedema without monoclonal gammopathy mimicking angioedema, rapidly developing and responding to steroid treatment.en_US
dc.identifier.doi10.4274/turkderm.04809
dc.identifier.endpage30en_US
dc.identifier.issn1019-214X
dc.identifier.issn1308-6294
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84964061363en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage28en_US
dc.identifier.urihttps://doi.org/10.4274/turkderm.04809
dc.identifier.urihttps://hdl.handle.net/11616/97279
dc.identifier.volume50en_US
dc.identifier.wosWOS:000378113100007en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.publisherDeri Zuhrevi Hastaliklar Dernegien_US
dc.relation.ispartofTurkderm-Turkish Archives of Dermatology and Venerologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectScleromyxedemaen_US
dc.subjectangioedemaen_US
dc.subjecttreatmenten_US
dc.titleA case of angioedema-like atypic scleromyxedema responding to treatment with steroiden_US
dc.typeArticleen_US

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