纯巨核细胞再生障碍性血小板减少症47例分析

Analysis in 47 Cases of Acquired Amegakaryocytic Thrombocy-topenic Purpura

回顾性分析了47例纯巨核细胞再生障碍性血小板减少症的诊断、鉴别诊断及本病实质问题。通过分析进一步明确本病的诊断标准,以及应与ITP和再障鉴别。并认为本病可能是不典型再障的一个特殊类型或再障早期。至于该病是否能转归为再障,还需作长期随访观察,积累更多的资料。

The diagnosis, differentiation and other principal problems of acguired amegakaryocytic thrombocy tiopenic purpura in 47 cases are reviewed. Byfurther analysing. We clariiy the diagnositio standord of thei diseose and it's differentiation to thrombocytopenic purpura and aplastic anemia. We comsider that it might fe a special type of atypical aplaotio anemia or the early stage of aplastio anemia. It needs long terms observation of flloioing-up and more accumulated data to determine if it can totally transform aplastie anemia.