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一名骨髓增生异常综合征患者在接受细胞因子(粒细胞集落刺激因子和促红细胞生成素)与大剂量甲泼尼龙联合治疗后,实现了持续的三系造血恢复且异常染色体克隆消失。

Sustained trilineage recovery and disappearance of abnormal chromosome clone in a patient with myelodysplastic syndrome following combination therapy with cytokines (granulocyte colony-stimulating factor and erythropoietin) and high-dose methylprednisolone.

作者信息

Imai Y, Fukuoka T, Nakatani A, Ohsaka A, Takahashi A

机构信息

Department of Internal Medicine, Hitachi General Hospital, Ibaraki, Japan.

出版信息

Br J Haematol. 1996 Apr;93(1):146-50. doi: 10.1046/j.1365-2141.1996.460997.x.

Abstract

We report a case of hypoplastic myelodyplastic syndrome (MDS) (refractory anemia (RA)) in which sustained trilineage haematological response and persistent disappearance of an abnormal chromosome clone were achieved after treatment with combination therapy of cytokines (granulocyte colony-stimulating factor (G-CSF) and erythropoietin (Epo)) and methylprednisolone (mPSL) pulse dose. The patient's haematological recovery was rapid and maintained even after cessation of the therapy. In addition, the predominant chromosome clone 13q- in bone marrow cells disappeared in the fourth week. The patient's improved bone marrow haemopoiesis and disappearance of the abnormal chromosome has continued to the present, 13 months after treatment. The occurrence of both trilineage response and abnormal chromosome disappearance in MDS patients treated with cytokine(s) or steroids is rare. Combination therapy might therefore be advantageous in MDS.

摘要

我们报告了一例低增生性骨髓增生异常综合征(MDS)(难治性贫血(RA))患者,经细胞因子(粒细胞集落刺激因子(G-CSF)和促红细胞生成素(Epo))联合甲基强的松龙(mPSL)脉冲剂量治疗后,获得了持续的三系血液学反应以及异常染色体克隆的持续消失。患者的血液学恢复迅速,即使在治疗停止后仍得以维持。此外,骨髓细胞中占主导地位的染色体克隆13q-在第四周消失。患者骨髓造血功能改善以及异常染色体消失的情况一直持续至今,即治疗后13个月。在接受细胞因子或类固醇治疗的MDS患者中,出现三系反应和异常染色体消失的情况较为罕见。因此,联合治疗可能对MDS有益。

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