首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >Acute T-lymphoblastic leukemia relapsed with the character of myeloidatural killer cell precursor phenotype: a case report.
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Acute T-lymphoblastic leukemia relapsed with the character of myeloidatural killer cell precursor phenotype: a case report.

机译:急性T淋巴细胞白血病复发,具有髓样/自然杀伤细胞前体表型特征:1例病例报告。

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摘要

The leukemic lymphoblasts of a patient expressed CD7, CD13, CD33, CD34, HLA-DR and cytoplasmic CD3varepsilon. He was diagnosed with acute lymphoblastic leukemia (ALL), and successfully treated with a conventional chemotherapy for ALL. The disease relapsed three times, and the character of the cells gradually altered, i.e. CD56 expression increased and CD13, CD7 and cCD3 epsilon decreased. The phenotype of the relapsed ALL was, therefore, compatible with myeloidatural killer cell precursor acute leukemia (M/NK-AL). Some of M/NK-AL may be closely related with T/myeloid-biphenotypic pro-T blasts, and both types of acute leukemia may develop a tendency to express myeloid antigens, and they may belong to the category of immature T lymphoid precursors.
机译:病人的白血病淋巴母细胞表达CD7,CD13,CD33,CD34,HLA-DR和细胞质CD3varepsilon。他被诊断出患有急性淋巴细胞白血病(ALL),并通过常规化学疗法成功治疗了ALL。该疾病复发了三遍,并且细胞的特征逐渐改变,即CD56表达增加并且CD13,CD7和cCD3ε降低。因此,复发的ALL的表型与髓样/天然杀伤细胞前体急性白血病(M / NK-AL)相容。一些M / NK-AL可能与T /髓样双表型pro-T母细胞密切相关,并且两种类型的急性白血病都可能表达髓样抗原,并且可能属于未成熟T淋巴样前体。

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