| Literature DB >> 24315227 |
M Versini1, F Mantoux, K Angeli, T Passeron, J-P Lacour.
Abstract
BACKGROUND: Sneddon-Wilkinson disease (SWD) is a rare chronic neutrophilic dermatosis. The first-line treatment is dapsone but resistance to treatment may sometimes pose a challenge. CASE REPORT: We report a multidrug-resistant patient who responded dramatically before gradually losing response to infliximab and then etanercept. Complete remission was again obtained with adalimumab. DISCUSSION: Our case confirms the previously reported dramatic efficacy of anti-TNF biological agents in recalcitrant SWD but highlights the possibility of subsequent loss of response. Furthermore, it illustrates the efficacy of adalimumab in this indication.Entities:
Keywords: Adalimumab; Anti-TNF; Biothérapie anti-TNFalpha; Dermatose neutrophilique; Maladie de Sneddon-Wilkinson; Neutrophilic dermatosis; Sneddon-Wilkinson disease
Mesh:
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Year: 2013 PMID: 24315227 DOI: 10.1016/j.annder.2013.07.012
Source DB: PubMed Journal: Ann Dermatol Venereol ISSN: 0151-9638 Impact factor: 0.777