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低剂量重组人促红细胞生成素治疗再生障碍性骨髓增生异常综合征合并染色体异常患者时贫血状况持续改善。

Sustained improvement in anemia with low-dose recombinant human erythropoietin therapy in a patient with hypoplastic myelodysplastic syndrome and chromosomal abnormalities.

作者信息

Tamai Y, Takami H, Nakahata R, Kariya K, Munakata A

机构信息

First Department of Internal Medicine, Hirosaki University School of Medicine.

出版信息

Intern Med. 1998 Mar;37(3):320-3. doi: 10.2169/internalmedicine.37.320.

Abstract

We present a case report of a 55-year-old male patient with hypoplastic myelodysplastic syndrome (MDS, refractory anemia) in which a good response to recombinant human erythropoietin (rhEPO) has been maintained for more than 60 months. There is with no evidence of progression to high risk MDS or acute leukemia, although he was predicted to be a low-responder to rhEPO therapy because of very high serum EPO levels (5,260 mU/ml), a history of multiple transfusions, chromosomal abnormalities (47,XY,+8) and severe thrombocytopenia. Since he received rhEPO with no adverse effects, it may be valuable to try rhEPO treatment at least one time for low-risk MDS patients, depending on red cell transfusion requirements.

摘要

我们报告一例55岁男性低增生性骨髓增生异常综合征(MDS,难治性贫血)患者,其对重组人促红细胞生成素(rhEPO)保持良好反应已超过60个月。尽管由于血清促红细胞生成素水平非常高(5260 mU/ml)、多次输血史、染色体异常(47,XY,+8)和严重血小板减少症,预计他对rhEPO治疗反应较差,但并无进展为高危MDS或急性白血病的证据。由于他接受rhEPO治疗无不良反应,根据红细胞输血需求,对低危MDS患者至少尝试一次rhEPO治疗可能是有价值的。

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