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Sustained remission of MDS overt leukemia associated with abrupt discontinuation of immunosuppression following relapse after the second course of allogeneic hematopoietic stem cell transplantation

机译:异基因造血干细胞移植第二个疗程复发后MDS持续性白血病缓解与免疫抑制突然终止相关

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The case of a 32-year-old female with relapsed myelodysplastic syndrome (MDS) after second course of allogeneic transplantation is described. The peripheral blood stem cell transplantation was performed as early as 3 months after the initial bone marrow transplantation because of rejection and relapse; however, the patient again relapsed 2 months later. Immediate discontinuation of cyclosporine resulted in the progression of pancytopenia and the development of high fever, liver dysfunction and skin eruption. The patient was then treated with dexamethasone, which successfully stabilized these symptoms. After these clinical events, a dramatic hematological response was obtained; the blast rate was reduced from 10.6 to 0% in bone marrow aspiration, and pancytopenia was restored to normal levels. Moreover, fluorescence in situ hybridization analyses with X and Y chromosome-specific probes revealed that hematopoietic precursor cells were predominantly of donor origin. The patient subsequently received donorlymphocyte infusion (DLI) from the original donor. Currently, 2 years after DLI, the patient continues to be in remission.
机译:描述了异基因移植第二个疗程后复发性骨髓增生异常综合症(MDS)的32岁女性的病例。由于排斥和复发,外周血干细胞移植最早在最初的骨髓移植后3个月进行。但是,患者在两个月后再次复发。立即停用环孢菌素会导致全血细胞减少症的发展以及高烧,肝功能障碍和皮肤疹的发展。然后用地塞米松治疗该患者,该药物成功稳定了这些症状。在这些临床事件之后,获得了惊人的血液学反应。骨髓抽吸的爆炸率从10.6%降至0%,全血细胞减少症恢复了正常水平。此外,用X和Y染色体特异性探针进行的荧光原位杂交分析表明,造血前体细胞主要来自供体。患者随后接受了原始供体的供体淋巴细胞输注(DLI)。目前,DLI后2年,患者仍在缓解。

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