Kolmos Eva Brøsted, Moth Henriksen Marie, Abildgaard Niels, Sindrup Søren Hein
Neurologisk Afdeling, Odense Universitetshospital.
Ugeskr Laeger. 2012 Oct 22;174(43):2635-6.
CANOMAD is a rare syndrome of chronic ataxic polyneuropathy, ophtalmoplegia, IgM paraprotein, cold agglutinins and anti-disialosyl antibodies. We present a case of a 65-year-old woman with clinical and electrophysiological features of chronic sensory polyneuropathy and diplopia. Serum samples from the patient contained IgM paraprotein and anti-GM2-antibodies. Treatment with intravenous immunoglobulins resulted in an improvement of the patient's diplopia and polyneuropathy. The case shows the importance of considering CANOMAD as a cause of diplopia in patients with chronic sensory polyneuropathy.
慢性共济失调性多神经病、眼肌麻痹、IgM 副蛋白、冷凝集素和抗二唾液酸基抗体综合征(CANOMAD)是一种罕见综合征。我们报告一例 65 岁女性病例,该患者具有慢性感觉性多神经病和复视的临床及电生理特征。患者血清样本中含有 IgM 副蛋白和抗 GM2 抗体。静脉注射免疫球蛋白治疗后,患者的复视和多神经病症状有所改善。该病例表明,对于患有慢性感觉性多神经病的复视患者,应考虑 CANOMAD 作为病因的重要性。