Abstract

Schnitzler syndrome (SS) is a rare autoinflammatory disorder characterized by a chronic urticarial rash and a monoclonal immunoglobulin M gammopathy, accompanied by recurrent fever, lymphadenopathy, arthralgia or arthritis, hepato- or splenomegaly and elevated levels of markers of systemic inflammation. Because patients often present to various specialists with different symptoms the syndrome is often undiagnosed, and it can take years before the correct diagnosis is made. Treatment with interleukin-1 receptor antagonists has a rapid effect on SS.
Bidragets oversatte titelSchnitzler syndrome is a diagnostic challenge
OriginalsprogDansk
TidsskriftUgeskrift for Laeger
Vol/bind177
Udgave nummer30
ISSN0041-5782
StatusUdgivet - 20 jul. 2015

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