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MDS是以难治性贫血和(或)伴有其他血细胞减少,骨髓造血干细胞功能异常的一组综合征,其临床和血液学变化多端,而缺乏特异性。为进一步探讨临床及血液学特征,作者对1982～1989年国内公开发表的有关论文29篇,计933例,进行综合分析,以提高对MDS规律性认识。一、一般资料 1.资料来源:采用FAB分型的MDS和白血病前期(白前)的资料。 2.性别和年龄:统计813例,其中男457例、
MDS is refractory anemia and (or) associated with other cytopenias, bone marrow hematopoietic stem cell dysfunction group of syndromes, its clinical and hematological changes in many, but the lack of specificity. To further explore the clinical and hematological characteristics, the author of the 1982 ~ 1989 published 29 domestic papers, including 933 cases, a comprehensive analysis to improve the understanding of regularity of MDS. First, the general information 1. Source: using FAB type MDS and pre-leukemia (white) data. Gender and age: Statistics 813 cases, including 457 males,