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首页> 外文期刊>Pathology Research and Practice >Transformation of primary myelofibrosis with 20q- in Philadelphia-positive acute lymphoblastic leukemia: Case report and review of literature
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Transformation of primary myelofibrosis with 20q- in Philadelphia-positive acute lymphoblastic leukemia: Case report and review of literature

机译:费城阳性急性淋巴细胞白血病中20q-原发性骨髓纤维化的转化:病例报告和文献复习

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摘要

A 56-year-old male with chronic idiopathic myelofibrosis and cytogenetic finding of 20q- after a period of 10 months developed acute Philadelphia-positive lymphoblastic leukemia. Immunophenotyping of peripheral blood by flow cytometry showed HLA-DR, CD34, CD19, CD22, CD10, CD33, and CD11b positivity. Cytogenetic analysis revealed the presence of 20q- and Philadelphia chromosome t(9;22)(q34:q11) at the time of disease transformation to ALL. The JAK2V617F mutation was not found. This is a very rare case of simultaneous presence of two cytogenetics abnormalities and evolution of primary idiopathic myelofibrosis to Philadelphia-positive acute lymphoblastic leukemia.
机译:一名56岁的男性,患有慢性特发性骨髓纤维化,在10个月的时间里发现了20q-的细胞遗传学特征,发展为急性费城阳性淋巴细胞白血病。通过流式细胞术对外周血进行免疫分型显示HLA-DR,CD34,CD19,CD22,CD10,CD33和CD11b阳性。细胞遗传学分析显示,在疾病转化为ALL时,存在20q-和费城染色体t(9; 22)(q34:q11)。找不到JAK2V617F突变。这是同时存在两种细胞遗传学异常以及原发性特发性骨髓纤维化发展为费城阳性急性淋巴细胞性白血病的极少数情况。

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