Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment

被引:32
作者
Campagnolo, Marta [1 ]
Ferrari, Sergio [2 ]
Torre, Chiara Dalla [1 ]
Cabrini, Ilaria [2 ]
Cacciavillani, Mario [3 ]
Lucchetta, Marta [1 ]
Ruggero, Susanna [1 ]
Toffanin, Elisabetta [1 ]
Cavallaro, Tiziana [2 ]
Briani, Chiara [1 ]
机构
[1] Univ Padua, Dept Neurosci Sci NPSRR, I-35128 Padua, Italy
[2] Univ Verona, Dept Neurol & Movement Sci, I-37100 Verona, Italy
[3] CEMES, EMG Unit, Padua, Italy
关键词
Myelin-associated glycoprotein (MAG); Sulfatide; Polyneuropathy; Demyelinating; Indirect immunofluorescence; Rituximab; NEURAL IGM ANTIBODIES; NEUROPATHY; DISEASE;
D O I
10.1016/j.jneuroim.2015.02.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IgM paraproteins often present reactivity to myelin-associated glycoprotein (MAG) and sulfatide. We describe the clinical and neurophysiological findings, and therapy response in 21 patients with IgM paraproteinemic neuropathy (15 with anti-MAG antibodies, 1 with anti-sulfatide antibodies, and 5 with both reactivity), and in 2 with anti-sulfatide positivity and no hematological disease. All patients complained of sensory symptoms, the majority had demyelinating neuropathy. Indirect immunofluorescence on human normal sural nerves disclosed different staining patterns. Eight of 13 patients (6 anti-MAG, 1 anti-sulfatide, 1 both anti-sulfatide and anti-MAG antibodies) improved after Rituximab. IVIg, steroids and plasma-exchange were also administered with different responses. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 4
页数:4
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