慢性骨髓性白血病伴获得性c-kit激活突变和短暂性骨髓肥大细胞增多症。

Roberto Cairoli, Giovanni Grillo, Alessandro Beghini, Giorgia Cornacchini, Lidia Larizza, Enrica Morra
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引用次数: 9

摘要

c-kit基因突变在骨髓增生性疾病中有报道。我们在此报告一例Ph+ (b2a2)慢性髓性白血病,在病程中,表现出不寻常的骨髓肥大细胞浸润。在随访期间对常规冷冻保存的DNA进行c-kit基因突变筛查,证明d816y激活突变是一种额外的遗传异常。甲磺酸伊马替尼治疗导致BCR-ABL/ABL比率大幅下降,并且没有c-kit突变。在这种情况下,叠加的c-kit突变可能是短暂性骨髓肥大细胞增多症的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic myelogenous leukemia with acquired c-kit activating mutation and transient bone marrow mastocytosis.

Mutations of the c-kit gene have been reported in myeloproliferative disorders. We describe here a case of Ph+ (b2a2) chronic myelogenous leukemia that, during the course of disease, showed an unusual bone marrow mast-cell infiltration. A mutational screening for the c-kit gene, performed on DNA routinely cryopreserved during the follow-up, evidenced the D816Y-activating mutation as an additional genetic abnormality. Treatment with imatinib mesylate resulted in a substantial decrease of the BCR-ABL/ABL ratio and in the absence of c-kit mutation. It is likely that the superimposed c-kit mutation, in this case, may account for the transient bone marrow mastocytosis.

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