[Atypical scleromyxedema with a granulomatous histological pattern and delayed sclerosis].

Date publication

mai 2016

Journal

Annales de dermatologie et de venereologie

Auteurs

Membres identifiés du Cancéropôle Est :
Pr CRIBIER Bernard

Tous les auteurs :
de Cambourg G, Goussot R, Wettlé C, Cribier B

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/26969478

Résumé

Papular mucinosis is characterised by primary mucin deposition in the dermis. The classification distinguishes between the localised form and the systemic form, which alone can result in complications, but this classification occasionally proves to be inadequate. Herein we report the progression of papular mucinosis, initially atypical due to the absence of cutaneous sclerosis and of misleading granulomatous histological features, which subsequently developed into characteristic scleromyxedema.

Référence

Ann Dermatol Venereol. 2016 May;143(5):382-6