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从1980～1984年10月,收治5例骨髓增生异常综合征,总结分析如下。结果与分析本文骨髓增生异常综合征5例中,男性4例,女性1例,年龄29～75岁。根据 FAB 协作组1982年建议的诊断标准分别是:难治性贫血 (RA)1例,原始细胞增多型难治性贫血(RAEB)8例,慢性粒单白血病(CMML)1例。转化型 RAEB 3例未列入本文。一、细胞增生情况:本文5例骨髓象皆为增生活跃,均有外周血细胞减少(红系、粒系
From 1980 to 1984 in October, admitted to 5 cases of myelodysplastic syndrome, summarized as follows. Results and Analysis In this paper, 5 cases of myelodysplastic syndrome, 4 males and 1 females, aged 29 to 75 years. According to the diagnostic criteria recommended by the FAB collaboration group in 1982, there were 1 refractory anemia (RA), 8 rheumatoid anemia (RAEB) and 1 chronic myelomonocytic leukemia (CMML). Three cases of transformed RAEB were not included in this article. First, the cell proliferation: 5 cases of bone marrow in this article are all hyperplasia, have peripheral blood cells decreased (erythroid, granulocytic