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Schnitzler's syndrome

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Schnitzler syndrome is a rare disorder characterized by chronic urticarial rashes and a monoclonal IgM gammopathy, variably combined with intermittent fever, arthralgia or arthritis, lymphadenopathy, hepatomegaly and/or splenomegaly, leukocytosis, and an elevated erythrocyte sedimentation rate (1).

Patients have an increased risk for Waldenstrom macroglobulinemia and amyloidosis.

Reference:

  • 1) Lipsker D, Veran Y, Grunenberger F, Cribier B, Heid E, Grosshans E. The Schnitzler's syndrome: four new cases and review of the literature. Medicine 2001;80: 37-44.
  • 2) de Koning HD, Bodar EJ, van der Meer JWM, Simon A. Schnitzler's Syndrome Study Group. Schnitzler's syndrome: beyond the case reports: review and followup of 94 patients with an emphasis on prognosis and treatment. Semin Arthritis Rheum 2007;37:137-48

 


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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