首页> 外文期刊>Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology >Five-month marrow aplasia in a child with refractory acute myeloid leukemia: successful management with continuous granulocyte support and reduced-intensity conditioning followed by matched unrelated bone marrow transplantation.
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Five-month marrow aplasia in a child with refractory acute myeloid leukemia: successful management with continuous granulocyte support and reduced-intensity conditioning followed by matched unrelated bone marrow transplantation.

机译:难治性急性髓细胞性白血病患儿五个月的骨髓发育不全:持续的粒细胞支持和降低的强度调节,然后进行相配的无关的骨髓移植,可成功治疗。

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摘要

A 10-year-old girl diagnosed with acute myeloid leukemia FAB M4 failed to achieve remission following several courses of induction chemotherapy. From the first course of chemotherapy the patient had continuous marrow aplasia, managed by a total of 57 granulocyte transfusions. After reinduction and reduced-intensity conditioning including fludarabine, Campath-1H, and melphalan, the patient received unmanipulated marrow from an HLA-matched unrelated donor. Leukocyte and platelet engraftment was observed on day +18 and +50, respectively. Graft-versus-host disease did not occur. The patient is alive and well in complete remission 18 months after transplantation with complete donor chimerism.
机译:一名经过诊断的急性髓性白血病FAB M4的10岁女孩在经过数次诱导化疗后均未获得缓解。从化疗的第一个疗程开始,患者就患有连续性骨髓发育不全,总共进行了57次粒细胞输血。进行减氟和强度降低的调理(包括氟达拉滨,Campath-1H和美法仑)后,患者从HLA匹配的无关供者那里接受了未操纵的骨髓。在第+18和+50天分别观察到白细胞和血小板植入。没有发生移植物抗宿主病。移植后18个月,患者完全存活,并且完全供体嵌合。

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