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粒细胞集落刺激因子、促红细胞生成素和环孢素A治疗后,一名对抗淋巴细胞球蛋白耐药的重型再生障碍性贫血患者出现持续三系反应:恢复与血清碱性磷酸酶显著升高相关。

Sustained trilineage response in a patient with ALG-resistant severe aplastic anaemia after treatment with G-CSF, erythropoietin and cyclosporin A: association of recovery with marked elevation of serum alkaline phosphatase.

作者信息

Weide R, Lyttelton M, Samson D, Görg C, Köppler H, Pflüger K H, Havemann K

机构信息

Department of Haematology/Oncology, Philipps University, Marburg, Germany.

出版信息

Br J Haematol. 1993 Nov;85(3):608-10. doi: 10.1111/j.1365-2141.1993.tb03355.x.

Abstract

Aplastic anaemia is characterized by multilineage bone marrow failure resulting in pancytopenia. We have successfully treated a young woman with severe aplastic anaemia (SAA) who was resistant to antilymphocyte globulin (ALG) and corticosteroids, with a combination therapy consisting of erythropoietin, cyclosporin A and granulocyte-colony stimulating factor (G-CSF). The patient received erythropoietin and CSA for a period of 10 months without success before G-CSF treatment was started. After 6 weeks of G-CSF therapy she responded with a sustained trilineage recovery. This suggests that immunosuppression together with haemopoietic growth factors may be an effective treatment in patients with SAA who are ALG resistant and cannot be treated by BMT.

摘要

再生障碍性贫血的特征是多系骨髓衰竭导致全血细胞减少。我们成功地用促红细胞生成素、环孢素A和粒细胞集落刺激因子(G-CSF)联合治疗了一名对抗淋巴细胞球蛋白(ALG)和皮质类固醇耐药的重症再生障碍性贫血(SAA)年轻女性。该患者在开始G-CSF治疗前接受促红细胞生成素和环孢素A治疗10个月均未成功。G-CSF治疗6周后,她出现持续的三系血细胞恢复。这表明免疫抑制与造血生长因子联合使用可能是治疗对ALG耐药且无法进行骨髓移植治疗的SAA患者的有效方法。

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