Plasmablastic Multiple Myeloma Masquerading Leukemia in an Immunocompetent Patient

A. Anand, Smita Singh, K. Agarwal
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Abstract

Multiple myeloma (MM) is a plasma cell neoplasm accounting for 1% of all malignancies. It is characterized by a monoclonal malignant proliferation of plasma cells accompanied by an increase in M-protein. Plasmablastic myeloma represents 5-15% of the cases of multiple myeloma. This morphology of a MM is an independent predictor of poor survival. Plasmablastic myeloma tends to have worse outcomes than other plasma cell dyscrasias. The median survival of these patients is around 1.9 years. Much of our knowledge on plasmablastic variant of MM is dependent on case reports and case series. Hence, an early identification of this aggressive variant of multiple myeloma and its differentiation from hematological malignancy like plasmablastic lymphoma is necessary for optimal patient management.
免疫功能正常患者的浆母细胞多发性骨髓瘤伪装白血病
多发性骨髓瘤(MM)是一种浆细胞肿瘤,占所有恶性肿瘤的1%。其特点是浆细胞单克隆恶性增殖伴m蛋白升高。浆母细胞骨髓瘤占多发性骨髓瘤病例的5-15%。MM的这种形态是生存不良的独立预测因子。浆母细胞骨髓瘤往往比其他浆细胞病变有更差的结果。这些患者的中位生存期约为1.9年。我们对MM的等离子体变体的了解大多依赖于病例报告和病例系列。因此,早期识别这种侵袭性多发性骨髓瘤,并将其与血液系统恶性肿瘤如浆母细胞淋巴瘤区分开来,对于优化患者管理是必要的。
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