发病机制
细胞减少
再生障碍性贫血
医学
骨髓
骨髓衰竭
髓系白血病
造血
免疫学
骨髓纤维化
骨髓增生异常综合症
贫血
髓样
癌症研究
内科学
干细胞
生物
遗传学
出处
期刊:Hematology
[Maney Publishing]
日期:2019-01-01
卷期号:24 (1): 559-566
被引量:75
标识
DOI:10.1080/16078454.2019.1642548
摘要
Aplastic anemia (AA) is a rare and life-threatening bone marrow failure (BMF) that results in peripheral blood cytopenia and reduced bone marrow hematopoietic cell proliferation. The symptoms are similar to myelofibrosis, myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) making diagnosis of AA complicated. The pathogenesis of AA is complex and its mechanism needs to be deciphered on an individualized basis. This review summarizes several contributions made in trying to understand AA pathogenesis in recent years which may be helpful for the development of personalized therapies for AA.
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