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重型再生障碍性贫血患者骨髓移植的选择

Selection of patients for bone marrow transplantation in severe aplastic anemia.

作者信息

Camitta B M, Rappeport J M, Parkman R, Nathan D G

出版信息

Blood. 1975 Mar;45(3):355-63.

PMID:1090310
Abstract

Despite androgens and intensive supportive care, satisfactory survival in severe aplastic anemia remains at 20% or less. Histocompatible bone marrow transplantation can restore normal hematopoiesis in approximately 40% of similarly severe individuals. Delay of transplantation for 3 wk after diagnosis allows time for proper evaluation and for many spontaneous recoveries. Further delay increases risks of fatal complications and decreases chances for successful transplantation while the incidence of spontaneous remission declines. When available, early histocompatible bone marrow transplantation may be the treatment of choice for severe aplastic anemia.

摘要

尽管使用了雄激素并给予强化支持治疗,但严重再生障碍性贫血患者的满意生存率仍维持在20%或更低。组织相容性骨髓移植可使约40%病情同样严重的患者恢复正常造血。诊断后延迟3周进行移植可留出时间进行适当评估以及等待许多患者自发恢复。进一步延迟会增加致命并发症的风险,降低成功移植的几率,同时自发缓解的发生率也会下降。若有条件,早期组织相容性骨髓移植可能是严重再生障碍性贫血的首选治疗方法。

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