IgM骨髓瘤的不寻常表现。

Q3 Medicine
Ankur Jain, Paras Gupta, Ankita Jaiswal Govil, Sumita Chaudhry
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引用次数: 0

摘要

免疫球蛋白M (IgM)副蛋白血症通常与淋巴浆细胞性淋巴瘤(LPL)或Waldenström巨球蛋白血症(WM)相关。IgM副蛋白引起的表现包括高黏度、获得性凝血功能障碍、冷球蛋白血症、血管炎和冷抗体介导的自身免疫性溶血性贫血。这些表现在LPL/WM患者中所占比例不等。IgM骨髓瘤仅占所有骨髓瘤病例的0.5-1%。我们描述了一位中年女性,她表现为5C:冷球蛋白血症、凝血功能障碍(获得性血管性血友病)、冷自身免疫性溶血性贫血、凝块(血管炎引起的血栓形成)和由IgM副蛋白引起的视力浑浊(高黏度综合征),但后来被诊断为IgM骨髓瘤。IgM是WM的重要鉴别诊断。目前的病例突出了这些诊断挑战及其治疗考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Unusual Presentation of IgM Myeloma.

Immunoglobulin M (IgM) paraproteinemia is usually associated with either lymphoplasmacytic lymphoma (LPL) or Waldenström's macroglobulinemia (WM). Manifestations due to IgM paraprotein include hyperviscosity, acquired coagulopathy, cryoglobulinemia, vasculitis, and cold antibody-mediated autoimmune hemolytic anemia. These manifestations are seen in variable percentage of patients with LPL/WM. IgM myeloma constitutes only 0.5-1% of all myeloma cases. We describe a middle-aged female who presented with 5C's: cryoglobulinemia, coagulopathy (acquired von Willebrand disease), cold autoimmune hemolytic anemia, clot (thrombosis due to vasculitis), and cloudy vision (hyperviscosity syndrome) attributable to IgM paraprotein, but was diagnosed later with IgM myeloma. IgM is an important differential diagnosis of WM. The current case highlights such diagnostic challenges and their therapeutic considerations.

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CiteScore
0.80
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509
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