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Peripheral stem cell transplantation in a child with amegakaryocytic thrombocytopenia.

机译:患有巨核细胞血小板减少症的儿童的外周干细胞移植。

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Congenital amegakaryocytic thrombocytopenia (CAMT) is an unusual cause of thrombocytopenia without radial or other congenital anomalies in the newborn. Generalized bone marrow dysfunction developing later in life has been reported. We present a 13-month-old girl who was diagnosed as having congenital amegakaryocytic thrombocytopenia and was successfully treated with allogeneic peripheral stem cell transplantation (PSCT) from her fully matched sibling donor. The neutrophil engraftment was on post transplant day 12 and platelet engraftment was on day 14. Her last hemogram revealed platelets of 168 x 10(9)/l 20 months post transplant.
机译:先天性巨核细胞性血小板减少症(CAMT)是新生儿血小板减少症的异常原因,无放射状或其他先天性异常。据报道,晚年发展为全身性骨髓功能障碍。我们介绍了一个13个月大的女孩,她被诊断患有先天性巨核细胞血小板减少症,并从她完全匹配的同胞供者那里成功接受了异基因外周血干细胞移植(PSCT)治疗。中性粒细胞植入在移植后第12天,而血小板植入在第14天。她的最后血流图显示移植后20个月血小板为168 x 10(9)/ l。

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