Schnitzler's syndrome - A novel hypothesis of a shared pathophysiologic mechanism with Waldenström's disease

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Abstract

Schnitzler's syndrome is an auto-inflammatory disorder which is characterized by two mandatory features: an urticarial rash and a monoclonal gammopathy. Although the pathophysiology of this syndrome is not yet fully understood, a role for interleukin-1 seems apparent. While this presumed link between interleukin-1 and the monoclonal gammopathy is not yet elucidated, a mutual factor in pathophysiology however seems likely. Here we present a novel hypothesis of a shared pathophysiologic mechanism between Schitzler's syndrome and monoclonal gammopathy.

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Van Leersum, F. S., Potjewijd, J., Van Geel, M., Steijlen, P. M., & Vreeburg, M. (2019). Schnitzler’s syndrome - A novel hypothesis of a shared pathophysiologic mechanism with Waldenström’s disease. Orphanet Journal of Rare Diseases, 14(1). https://doi.org/10.1186/s13023-019-1117-2

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