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通过异基因骨髓移植治疗范科尼贫血。

Fanconi's anemia treated by allogeneic marrow transplantation.

作者信息

Deeg H J, Storb R, Thomas E D, Appelbaum F, Buckner C D, Clift R A, Doney K, Johnson L, Sanders J E, Stewart P, Sullivan K M, Witherspoon R P

出版信息

Blood. 1983 May;61(5):954-9.

PMID:6338978
Abstract

Eight patients with Fanconi's anemia were given cyclophosphamide alone (seven patients) or combined with procarbazine and antithymocyte globulin (one patient) followed by marrow grafts from HLA-identical siblings. All patients had engraftment. Seven developed acute and three chronic graft-versus-host disease (GVHD). Three patients died with GVHD and infectious complications (days 19, 56, and 82) and one with an intracerebral hemorrhage (day 540). Four patients are surviving 647-3435 days after grafting, two are well, and two have chronic GVHD that is improving. These results show that Fanconi's anemia can be treated successfully by allogeneic marrow transplantation.

摘要

8例范可尼贫血患者单独接受环磷酰胺治疗(7例),或联合丙卡巴肼和抗胸腺细胞球蛋白治疗(1例),随后接受来自 HLA 相同同胞的骨髓移植。所有患者均实现植入。7例发生急性移植物抗宿主病(GVHD),3例发生慢性GVHD。3例患者死于GVHD和感染并发症(分别在第19、56和82天),1例死于脑出血(第540天)。4例患者在移植后647 - 3435天存活,2例情况良好,2例慢性GVHD正在改善。这些结果表明,异基因骨髓移植可成功治疗范可尼贫血。

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