Polat, AysegulKAPICIOĞLU, YELDASahin, NURHANYilmaz, Mikail2020-10-222020-10-222016-01-01Polat A., KAPICIOĞLU Y., Sahin N., Yilmaz M., -A case of angioedema-like atypic scleromyxedema responding to treatment with steroid-, TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, cilt.50, ss.28-30, 2016http://hdl.handle.net/20.500.12645/24784Lichen 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.A case of angioedema-like atypic scleromyxedema responding to treatment with steroidArticleWOS:0003781131000078496406136310.4274/turkderm.04809