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A case of severe aplastic anemia secondary to treatment with lenalidomide for multiple myeloma.

机译:来那度胺治疗多发性骨髓瘤继发严重再生障碍性贫血一例。

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Lenalidomide is an important contemporary treatment option for patients with multiple myeloma (MM). Rare instances of autoimmune conditions have been observed in association with its use. Although moderate myelosuppression is not uncommonly seen in patients treated with lenalidomide, aplastic anemia has not previously been reported to be associated with this agent. We describe a case of severe aplastic anemia (AA) that was probably induced by lenalidomide. A 64-year-old male patient developed progressive pancytopenia three weeks into therapy with lenalidomide for his relapsed MM. A bone marrow aspirate and biopsy confirmed the diagnosis of AA and suggested the existence of an immunological reaction at the level of marrow. A gradual spontaneous recovery of normal hematopoiesis followed after the lenalidomide discontinuation.
机译:来那度胺是多发性骨髓瘤(MM)患者的重要现代治疗选择。已经观察到罕见的自身免疫性疾病及其用途。尽管在来那度胺治疗的患者中很少见到中等程度的骨髓抑制,但先前尚未报道再生障碍性贫血与该药物有关。我们描述了一个可能由来那度胺诱导的严重再生障碍性贫血(AA)病例。一名64岁的男性患者在接受来那度胺治疗的MM复发三周后出现进行性全血细胞减少症。骨髓穿刺活检证实了AA的诊断,并提示在骨髓水平存在免疫反应。来那度胺停用后,逐渐逐渐恢复正常的造血功能。

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