Geissler K
I. Medizinischen Universitätsklinik Wien.
Wien Med Wochenschr. 1991;141(9-10):201-4.
Ineffective hematopoiesis in MDS and evolution of acute leukemia in these patients are serious consequences of a neoplastic transformation at the stem cell level. The development of one or more cell clones is associated with morphological, cytogenetical and immunological aberrations and with changes in the normal stem cell pattern. For young people with MDS having an HLA identical donor bone marrow transplantation as the only curative approach so far is the treatment of choice. Younger people (less than 50 years) have a good chance to achieve complete remission by aggressive chemotherapy. In the majority of older people suffering from MDS treatment will be restricted to supportive measures. Recombinant hematopoietic growth factors can improve cytopenia in MDS.
骨髓增生异常综合征(MDS)中无效造血以及这些患者急性白血病的演变是干细胞水平肿瘤转化的严重后果。一个或多个细胞克隆的发展与形态学、细胞遗传学和免疫学异常以及正常干细胞模式的改变有关。对于患有MDS的年轻人来说,进行人类白细胞抗原(HLA)配型相同的供体骨髓移植是目前唯一的治愈方法,是首选治疗方式。较年轻的患者(小于50岁)通过积极化疗有很大机会实现完全缓解。在大多数患有MDS的老年人中,治疗将限于支持性措施。重组造血生长因子可改善MDS中的血细胞减少。