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作 者:Yang GAO Fei GAO Jimin SHI Huarui FU He HUANG Yanmin ZHAO
机构地区:[1]Bone Marrow Transplantation Center,the First Affiliated Hospital,School of Medicine,Zhejiang University,Hangzhou 310003,China [2]Institute of Hematology,Zhejiang University,Hangzhou 310058,China [3]Zhejiang Engineering Laboratory for Stem Cell and Immunotherapy,Hangzhou 310058,China
出 处:《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》2021年第8期695-700,共6页浙江大学学报(英文版)B辑(生物医学与生物技术)
基 金:supported by the National Natural Science Foundation of China (No. 81670148);the Health Science and Technology Project of Zhejiang Province (No. 2012KYB079), China。
摘 要:Pure red cell aplasia(PRCA) is a well-recognized complication of ABO major mismatched allogeneic hematopoietic stem cell transplantation(allo-HSCT), with a reported incidence of 10% – 20%(Zhidong et al., 2012;Busca et al., 2018). It is clinically characterized by anemia, reticulocytopenia,and the absence of erythroblasts in a normal-appearing bone marrow biopsy(Shahan and Hildebrandt, 2015).The mechanism for PRCA has been presumed to be persistence of recipient isoagglutinins, produced by residual host B lymphocytes or plasma cells。
关 键 词:ABO al. HEMATOPOIETIC
分 类 号:R556.5[医药卫生—血液循环系统疾病]
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