5 years ago

Vasculitis and IgA monoclonal gammopathy of cutaneous significance

J-D. Bouaziz, M. Rybojad, E. Oksenhendler, F. Cordoliani, M. Battistella, M. Jachiet, L. Rousset, M. Bagot, E. Pillebout
IgA vasculitis (Henoch-Schonlein purpura) is a small vessel systemic vasculitis involving IgA immunoglobulin polyclonal activation1. Monoclonal gammopathy of cutaneous significance is a subgroup of monoclonal gammopathy with skin disease, without myeloma or lymphoproliferative disorder2. We report 3 patients with vasculitis and IgA monoclonal gammopathy of cutaneous significance. Three men, 38, 37 and 50 years old, had a vascular purpura for more than 10 years with partial remission and frequent necrotic flares (Figure 1). This article is protected by copyright. All rights reserved.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1111/jdv.14683

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