Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
McGovern Medical School, Houston, Texas, USA.
Acta Haematol. 2021;144(5):585-590. doi: 10.1159/000513925. Epub 2021 Mar 18.
CML is defined by the presence of an oncogenic fusion protein caused by a reciprocal translocation between chromosomes 9q and 22q. While our molecular understanding of CML pathogenesis has revolutionized drug development for this disease, we have yet to identify many predisposing factors for CML. Familial occurrence of CML has been rarely reported. Here, we describe 2 cases of CML in a 24-year-old woman and in her 73-year-old maternal great aunt. We describe genetic variants in these patients and report on their environmental exposures that may have contributed to CML pathogenesis. The possible familial association of these 2 cases of CML warrants further investigation into more definitive etiologies of this disease.
CML 是由 9 号染色体和 22 号染色体之间的相互易位导致的致癌融合蛋白的存在所定义的。虽然我们对 CML 发病机制的分子理解已经彻底改变了这种疾病的药物开发,但我们尚未确定许多导致 CML 的易患因素。家族性 CML 的发生很少有报道。在这里,我们描述了一名 24 岁女性及其 73 岁的外祖母的 CML 病例。我们描述了这些患者的基因变异,并报告了可能导致 CML 发病机制的环境暴露。这 2 例 CML 的可能家族关联性需要进一步调查,以确定该疾病的更明确病因。