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Treatment of pure red cell aplasia associated with multiple myeloma with biclonal gammopathy using cyclosporine A: a case report

机译:环孢素A治疗伴有双侧性丙种病的多发性骨髓瘤伴发的纯红细胞发育不良一例

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摘要

We reported a rare case of pure red cell aplasia in a 44-year-old man with multiple myeloma with biclonal gammophathy (IgG lambda and IgA lambda type) with severe anemia. After treatment with bortezomib, adriamycin, and dexamethasone, the patient achieved very good partial response with disappearance of monoclonal gammopathy. However, his anemia was not significantly improved. Bone marrow analysis revealed selective erythroid hypoplasia. Thus, cyclosporine A was administered, which resulted in a complete recovery from anemia. The present case may provide some insight into the pathogenesis of PRAC and malignant plasma cell disorder.
机译:我们报道了一名44岁的患有多发性骨髓瘤并伴有严重贫血的双侧性吞噬(IgGλ和IgAλ型)的多发性骨髓瘤的罕见病例。用硼替佐米,阿霉素和地塞米松治疗后,患者出现了很好的部分反应,伴有单克隆丙种球蛋白病消失。但是,他的贫血并没有明显改善。骨髓分析显示选择性红系发育不全。因此,施用环孢霉素A,导致贫血完全恢复。本病例可为PRAC和恶性浆细胞疾病的发病机理提供一些见识。

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