再生障碍性贫血及采用免疫抑制和骨髓移植治疗的重型再生障碍性贫血的病因发病机制
[Etiopathogenesis of aplastic anemia and of the severe form treated with immunosuppression and bone marrow transplantation].
作者信息
Dulley F L, Lotério H A, Massumoto C M, Llacer P E, Chamone D de A
出版信息
Rev Hosp Clin Fac Med Sao Paulo. 1989 Jul-Aug;44(4):167-70.
PMID:2696069
Abstract
Aplastic anemia is a condition characterized by bone marrow hipoplasia and pancytopenia. Various etiologic agents are related to the acquired form of this disease but in many cases the causative agents remain obscure. Severe aplastic anemia has been treated by immunosuppression and allogeneic marrow transplantation.
摘要
再生障碍性贫血是一种以骨髓发育不全和全血细胞减少为特征的病症。多种病因与该疾病的后天形式相关，但在许多情况下，致病因素仍不明确。重型再生障碍性贫血已通过免疫抑制和同种异体骨髓移植进行治疗。
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