Abstract：
:Schnitzler syndrome is characterized by monoclonal IgM gammopathy, urticaria, recurrent fever, evidence of inflammation, bone pain, and arthralgia, occasionally in combination with lymphadenopathy and/or hepatosplenomegaly. Only about 80 cases have been reported to date. Development of a hematological malignancy is the main complication. Recent reports of remissions induced by IL-1 receptor antagonist therapy shed new light on the pathophysiology of the disease.
journal_name
Joint Bone Spinejournal_title
Joint bone spineauthors
Soubrier Mdoi
10.1016/j.jbspin.2007.07.014subject
Has Abstractpub_date
2008-05-01 00:00:00pages
263-6issue
3eissn
1297-319Xissn
1778-7254pii
S1297-319X(08)00030-4journal_volume
75pub_type
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