摘要
再生障碍性贫血(AA)是由于物理、化学、生物或不明因素作用使骨髓造血干细胞和骨髓微环境严重受损,造成骨髓造血功能降低或衰竭,以全血细胞减少为主要表现的一组综合征。AA发病机理复杂,目前尚未完全明了,对AA病理机制的深入研究有利于提高AA的诊疗水平。本文就近年来AA发病机制及其治疗方面的进展作一综述。
Aplastic anemia(aplastic anemia,AA) is a blood disorder in which the bone marrow hematopoietic stem cells and bone marrow microenvironment were severely damaged cudsed by physical,chemical,biological,or unknown factors,resulting in reduced bone marrow function or failure,and manifesting mainly as pancytopenia.The pathogenesis is complicated and have not been still comprehensively understood.It will be benefit for the improvement of the diagnosis and treatment to elucidate the precise mechanism of AA.In this paper,recent progress in the pathogenesis and treatment of AA was reviewed.
出处
《四川解剖学杂志》
2011年第1期48-50,共3页
Sichuan Journal of Anatomy