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所有分裂的髓系细胞均存在染色体异常(46,XY,20q-)的慢性粒单核细胞白血病:粒细胞、单核细胞、红细胞和血小板共同的多能干细胞克隆起源的证据

Chronic myelomonocytic leukemia with a chromosome abnormality (46,XY,20q-) in all dividing myeloid cells: evidence for clonal origin in a multipotent stem cell common to granulocyte, monocyte, erythrocyte, and thrombocyte.

作者信息

Shinohara T, Takuwa N, Morishita K, Ieki R, Yokota J, Nakayama E, Asano S, Miwa S

出版信息

Am J Hematol. 1983 Nov;15(3):289-93. doi: 10.1002/ajh.2830150310.

Abstract

In a typical case of chronic myelomonocytic leukemia (CMML), a chromosome abnormality, 46,XY,20q-, was observed in all the dividing cells including up to 16-ploid cells in the bone marrow and the blood. As the mitotic figures could be easily seen not only in myelomonocytoid cells but also in erythroblasts in the bone marrow smear, it was concluded that all the cell lineages except lymphocytes had the abnormality. The present case will support the view that the leukemic process in CMML affects a multipotent stem cell rather than a granulocyte-monocyte committed stem cell.

摘要

在一例典型的慢性粒单核细胞白血病(CMML)中,在包括骨髓和血液中多达16倍体细胞在内的所有分裂细胞中均观察到染色体异常,即46,XY,20q-。由于不仅在骨髓涂片的粒单核样细胞中,而且在成红细胞中都能很容易地看到有丝分裂图像,因此得出结论,除淋巴细胞外的所有细胞谱系都有该异常。本病例将支持这样一种观点,即CMML中的白血病过程影响多能干细胞而非粒系-单核系定向干细胞。

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