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本文观察30例骨髓增生异常综合征(MDS)的网织红细胞的殊蛋白α:β肽链合成比率及其预后价值。本组男20例,女10例;年龄61—84岁,平均73岁,虽尚未用细胞毒药物治疗,但均依赖输血,观察时距最后一次输血至少3周。按FAB 分型,难治性贫血(RA)2例,环状铁粒幼稚细胞贫血(RAS)5例,原始细胞过多难治性贫血(RAEB)9例,转化中原始细胞过多难治性贫血(RAEB-T)6例,慢性粒、
This article observed 30 cases of myelodysplastic syndrome (MDS) reticulocyte repertoire protein α: β peptide synthesis ratio and prognostic value. The group of 20 males and 10 females; aged 61-84 years old, an average of 73 years old, although not yet treated with cytotoxic drugs, but all rely on blood transfusion, observed from the last blood transfusion for at least 3 weeks. According to FAB classification, refractory anemia (RA) in 2 cases, annular iron granulocyte blast cell anemia (RAS) in 5 cases, blaste blasts, refractory anemia (RAEB) in 9 cases, 6 cases of anemia (RAEB-T), chronic granulocyte,