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表现为髓系/自然杀伤细胞前体免疫表型特征的慢性髓性白血病急变期

Blast crisis of chronic myelogenous leukemia exhibiting immunophenotypic features of a myeloid/natural killer cell precursor.

作者信息

Murase T, Suzuki R, Tashiro K, Morishima Y, Nakamura S

机构信息

Department of Hematology, Toyota Memorial Hospital, Japan.

出版信息

Int J Hematol. 1999 Feb;69(2):89-91.

Abstract

We report a patient with Philadelphia chromosome (Ph1)-positive chronic myelogenous leukemia (CML) which transformed into blast crisis bearing the immunophenotypic features similar to those of the myeloid/natural killer (NK) cell precursor leukemia we proposed previously. Using a CD45 blast gating method, the myeloperoxidase-negative blasts were positive for CD7, CD13, CD33, CD34, CD56, and HLA-DR, but no other lymphoid antigens. Southern blot analysis showed germ line T cell receptor beta and delta genes and immunoglobulin heavy and light chain genes. Although NK cell blastic transformation with Ph1 positive CML has been reported in a single patient, this is, to our knowledge, the first report of CML blast crisis of myeloid/NK cell precursor origin.

摘要

我们报告了1例费城染色体(Ph1)阳性的慢性粒细胞白血病(CML)患者,该患者转化为原始细胞危象,其免疫表型特征与我们之前提出的髓系/自然杀伤(NK)细胞前体白血病相似。采用CD45原始细胞设门法,髓过氧化物酶阴性的原始细胞CD7、CD13、CD33、CD34、CD56和HLA-DR呈阳性,但无其他淋巴样抗原。Southern印迹分析显示种系T细胞受体β和δ基因以及免疫球蛋白重链和轻链基因。虽然在1例患者中曾报道过Ph1阳性CML发生NK细胞原始细胞转化,但据我们所知,这是首例起源于髓系/NK细胞前体的CML原始细胞危象报告。

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