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Nonsecretory primary plasma cell leukemia successfully treated with VAD and MP therapy

机译:Nonsecretory初级血浆细胞白血病用VAD和MP疗法成功治疗

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A 78-year-old woman was admitted to our hospital because of lumbago and appetite loss. Blood analysis revealed anemia, hypercalcemia and circulating plasma cells. Bone marrow aspiration showed an elevated ratio (43%) of plasma cells, which expressed CD38 in the absence of CD19 and CD56 expression. Spinal MR imaging revealed multiple compression fractures and suggested diffuse invasion of plasma cells into the spinal bodies. No M-protein was detectable in serum or urine by immunoelectrophoresis and immunofixation, but cytoplasmic M-protein (IgG-kappa) was detected by enzyme antibody staining. On the basis of the history and data, nonsecretory primary plasma cell leukemia was diagnosed. First, the patient was given modified VAD therapy (vincristine, doxorubicin, and prednisolone) and complete remission was obtained. Then MP therapy (melphalan and prednisolone) was instituted, and remission has since been maintained for 11 months. Like many other cases of primary plasma cell leukemia, this case suggests that CD56 may act as an adhesion molecule between neoplastic plasma cells and bone marrow stromal cells. Our experience with this exceedingly rare case suggests the superiority of combination chemotherapy as an induction therapy and the effectiveness of MP therapy as maintenance therapy for this disease.
机译:由于腰痛和食欲损失,一名78岁的女子被院内入学。血液分析显示贫血,高钙血症和循环血浆细胞。骨髓抽吸显示升高的血浆细胞(43%)的血浆细胞,其在不存在CD19和CD56表达的情况下表达CD38。脊髓MR成像显示多重压缩骨折,并建议将血浆细胞的弥漫性侵入血浆中进入脊柱。通过免疫电泳和免疫混件在血清中或尿液中可检测到M蛋白,但通过酶抗体染色检测细胞质M蛋白(IgG-Kappa)。在历史和数据的基础上,诊断出非分泌原血浆细胞白血病。首先,给予患者修饰的VAD治疗(血管内,多柔比蛋白和泼尼松龙)并获得完全缓解。然后进行MP治疗(Melphalan和Prednisolone),并且已经保持了11个月以来的缓解。与许多其他血浆细胞白血病一样,这种情况表明CD56可以用作肿瘤血浆细胞和骨髓基质细胞之间的粘附分子。我们对此罕见的情况的经验表明,组合化疗的优越性是诱导治疗和MP治疗作为这种疾病的维持治疗的有效性。

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