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Le syndrome de Schnitzler (SdS) est une entité rare et méconnue qui fait partie des manifestations systémiques associées aux gammapathies monoclonales. Sa physiopathologie reste mystérieuse, même si plusieurs arguments suggèrent qu’il s’agisse d’un syndrome auto-inflammatoire de révélation tardive, acquis. Le SdS survient en moyenne vers 50 à 60ans et se manifeste par une éruption d’allure urticarienne...
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