Massive splenomegaly as the presenting feature of multiple myeloma in an elderly man

Vaibhav Mishra, A. Pandey, Deeksha Goyal, S. Chakrabarti
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Abstract

A 70-year-old man presented with generalized weakness, easy fatigability, and early satiety of 2-month duration. On examination, he had severe pallor and massive splenomegaly. Hematological investigations revealed bicytopenia with hypergammaglobulinemia and acute kidney injury. Bone marrow aspiration cytology was suggestive of plasma cell dyscrasia. Monoclonal protein peak (due to heavy chain of IgG type) was found on serum protein electrophoresis, and lambda light chains and IgG heavy chains were elevated on immunofixation. The patient was diagnosed as a case of multiple myeloma and was started on bortezomib–lenalidomide–dexamethasone regimen. After 7 months of chemotherapy, his spleen had regressed, and the patient had become asymptomatic. Presentation with massive splenomegaly is usually a feature of Waldenstrom's macroglobulinemia. However, rarely multiple myeloma may have extramedullary manifestations such as splenomegaly as the primary presenting feature.
老年男性多发性骨髓瘤的特征性表现为脾肿大
70岁男性,表现为全身无力,易疲劳,早期饱腹感持续2个月。经检查,患者面色严重苍白,脾肿大。血液学调查显示双氧体减少症伴高γ球蛋白血症和急性肾损伤。骨髓抽吸细胞学提示浆细胞病变。血清蛋白电泳发现单克隆蛋白峰(由于IgG型重链),免疫固定时λ轻链和IgG重链升高。患者被诊断为多发性骨髓瘤,并开始使用硼替佐米-来那度胺-地塞米松方案。化疗7个月后,脾脏退化,无症状。大量脾肿大通常是瓦尔登斯特罗姆巨球蛋白血症的一个特征。然而,罕见的多发性骨髓瘤可能有髓外表现,如脾肿大为主要表现特征。
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