医学
Diamond–Blackfan贫血
造血干细胞移植
再生障碍性贫血
干细胞
救世主兄弟
儿科
疾病
移植
内科学
贫血
肿瘤科
骨髓
化学
基因
核糖体
生物
核糖核酸
生物化学
遗传学
作者
Cristina Díaz de Heredia,Dorine Bresters,Lawrence Faulkner,Akif Yeşilipek,Brigitte Strahm,Maurizio Miano,Jean‐Hugues Dalle,Régis Peffault de Latour,Selim Corbacioglu
标识
DOI:10.1038/s41409-021-01449-w
摘要
Diamond Blackfan anemia (DBA) is a rare congenital syndrome presenting primarily as pure red cell aplasia with constitutional abnormalities and cancer predisposition. Established treatment options are corticosteroids, regular erythrocyte transfusions with iron chelation therapy, and hematopoietic stem cell transplantation (HSCT). To date, HSCT is the only definitive curative treatment for the hematological phenotype of DBA, but there is little experience with its use. Given the rarity of the disease and its unique features, an expert panel agreed to draw up a set of recommendations on the use of HSCT in DBA to guide clinical decision-making and practice. The recommendations address indications, pretransplant patient evaluation, donor selection, stem cell sources, conditioning regimens, prophylaxis of rejection and graft versus host disease, and post-transplant follow-up.
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