将all转换为aml是一种罕见的现象

M. Kishore, Vijay Kumar, S. Marwah, A. Nigam
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引用次数: 0

摘要

在所有急性白血病中,急性淋巴细胞白血病(all)的发病率是急性髓性白血病(AML)的5倍。从ALL到AML的血统转换是非常罕见的。谱系切换是在白血病病例中注意到的一种现象,最初诊断的白血病谱系(淋巴/髓系)复发时出现相反的谱系。在这里,我们报告一个10岁男孩的病例,他最初被诊断为ALL, 4年后复发,表现为AML。母细胞形态和免疫表型符合典型AML的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CONVERSION OF ALL TO AML: A RARE PHENOMENON
Among all acute leukemias, acute lymphoblastic leukemia (ALL) is five times more common than acute myeloid leukemia (AML). Lineage switch from ALL to AML is very rare. Lineage switching is a phenomenon noted in cases of leukemias where the initially diagnosed cases of leukemias of a lineage (lymphoid/myeloid) present with the opposite lineage at relapse. Here, we report the case of a 10-year-old male child who was initially diagnosed with ALL and on relapse after 4 years, presented with AML. The blast cell morphology and immunophenotype were consistent with the diagnosis of typical AML.
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