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Refractory urticaria and the importance of diagnosing Schnitzler’s syndrome

机译:难治性荨麻疹以及诊断施尼茨勒综合征的重要性

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摘要

A 52-year-old man presented with chronic urticaria that was refractory to standard chronic spontaneous urticaria (CSU) treatment. Over time, he developed systemic symptoms including fatigue, weight loss, arthralgia and bone pain. His laboratory investigations also became significant for microcytic anaemia, neutrophilia and elevated C reactive protein, erythrocyte sedimentation rate and IgE levels, in addition to an IgM monoclonal protein. He achieved only partial remission with typical medications for CSU including omalizumab, cyclosporine and cetirizine. After 6 years, his worsening symptoms and abnormal investigations led to a rare diagnosis of Schnitzler’s syndrome and a trial of the interleukin 1 receptor antagonist, anakinra, which caused a rapid and complete resolution of his symptoms.
机译:一名52岁男子患有慢性荨麻疹,令人难以忍受的标准慢性自发性荨麻疹(CSU)治疗。随着时间的推移,他开发了系统性症状,包括疲劳,减肥,关节痛和骨痛。除了IgM单克隆蛋白外,他的实验室研究还对微细胞贫血,中性粒细胞和升高的C反应蛋白,红细胞沉积率和IgE水平变得显着。他只取得了含有奥马拉姆,环孢菌素和甲基嗪的典型药物的部分缓解药物。 6年后,他的恶化症状和异常调查导致了对斯科尼茨勒综合征的罕见诊断,并对白细胞介素1受体拮抗剂,阿纳基拉的试验引起了他的症状的快速和完全解决。

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