Schnitzler Syndrome

An extremely rare condition manifested as monoclonal IMMUNOGLOBULIN M dysproteinemia without features of lymphoproliferative disease, but with chronic urticaria, fever of unknown origin, disabling bone pain, hyperostosis, and increased erythrocyte sedimentation rate.

Year introduced: 1998

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Tree Number(s): C20.683.780.640.700

MeSH Unique ID: D019873

All MeSH Categories
Diseases Category
Immune System Diseases
Immunoproliferative Disorders
Paraproteinemias
Monoclonal Gammopathy of Undetermined Significance
Schnitzler Syndrome