A case of angioedema-like atypic scleromyxedema responding to treatment with steroid
| Autor: | Ayşegül Polat, Yelda Kapicioglu, Nurhan Sahin, Mikail Yılmaz |
|---|---|
| Přispěvatelé: | ŞAHİN, NURHAN |
| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
medicine.medical_specialty
medicine.medical_treatment Dermatology lcsh:RC870-923 Steroid 030207 dermatology & venereal diseases 03 medical and health sciences 0302 clinical medicine stomatognathic system Scleromyxedema medicine lcsh:Dermatology skin and connective tissue diseases Angioedema integumentary system treatment business.industry angioedema lcsh:RL1-803 lcsh:Diseases of the genitourinary system. Urology stomatognathic diseases 030220 oncology & carcinogenesis Polat 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 2016 medicine.symptom business |
| Zdroj: | Türkderm, Vol 50, Iss 1, Pp 28-30 (2016) |
| Popis: | Lichen 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. |
| Databáze: | OpenAIRE |
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