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再生障碍性贫血的发病机制。

Pathogenesis of aplastic anemia.

作者信息

Wang Li, Liu Hong

机构信息

a Department of Hematology , Affiliated Hospital of Nantong University , Nantong , People's Republic of China.

出版信息

Hematology. 2019 Dec;24(1):559-566. doi: 10.1080/16078454.2019.1642548.

Abstract

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.

摘要

再生障碍性贫血(AA)是一种罕见且危及生命的骨髓衰竭(BMF),可导致外周血细胞减少和骨髓造血细胞增殖减少。其症状与骨髓纤维化、骨髓增生异常综合征(MDS)和急性髓系白血病(AML)相似,使得AA的诊断较为复杂。AA的发病机制复杂,其机制需要个体化解读。本综述总结了近年来在试图理解AA发病机制方面所做的一些贡献,这可能有助于开发AA的个性化治疗方法。

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