首页> 美国卫生研究院文献>BMJ Case Reports >Case Report: Acute inflammatory neuropathy with monoclonal anti-GM2 IgM antibodies, IgM-κ paraprotein and additional autoimmune processes in association with a diffuse large B-cell non-Hodgkin's lymphoma
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Case Report: Acute inflammatory neuropathy with monoclonal anti-GM2 IgM antibodies, IgM-κ paraprotein and additional autoimmune processes in association with a diffuse large B-cell non-Hodgkin's lymphoma

机译:病例报告:急性炎性神经病,伴有单克隆抗GM2 IgM抗体,IgM-κ副蛋白和其他自身免疫过程,并伴有弥漫性大B细胞非霍奇金淋巴瘤

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摘要

Lymphoproliferative disorders are often associated with autoimmune processes preceding or following the occurrence of a lymphoma. Here, we describe a patient with a history of recurrent diffuse large B-cell non-Hodgkin's lymphoma who suffered from an acute inflammatory neuropathy with specific monoclonal anti-GM2 IgM antibodies and associated IgM-κ paraprotein. It was possible in this case to prove that both, anti-GM2 IgM antibodies and IgM-κ paraprotein, share the same binding characteristic. In addition, the patient possibly suffered from an immune thrombocytopenia and an early-stage bullous pemphigoid with anti-BP-230 IgG antibodies. Intravenous immunoglobulin and plasmapheresis alleviated the acute neuropathy and thrombocytopenia, while the bullous pemphigoid has been aggravated. In summary, the simultaneous occurrence of multiple autoimmune processes was a sign of a dysfunctional immune system preceding the relapse of a B-cell non-Hodgkin's lymphoma.
机译:淋巴增生性疾病通常与淋巴瘤发生之前或之后的自身免疫过程有关。在这里,我们描述了一名患有复发性弥漫性大B细胞非霍奇金淋巴瘤病史的患者,该患者患有急性炎症性神经病,并伴有特定的单克隆抗GM2 IgM抗体和相关的IgM-κ副蛋白。在这种情况下,有可能证明抗GM2 IgM抗体和IgM-κ副蛋白都具有相同的结合特性。另外,该患者可能患有免疫性血小板减少症和抗BP-230 IgG抗体的早期大疱性类天疱疮。静脉注射免疫球蛋白和血浆置换可减轻急性神经病和血小板减少症,而大疱性类天疱疮则加重了病情。总之,多个自身免疫过程的同时发生是B细胞非霍奇金淋巴瘤复发之前免疫系统功能异常的迹象。

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