Campos L, Espinouse D, Felman P, Charrin C, Gentilhomme O, Germain D
Acta Haematol. 1986;76(2-3):169-72. doi: 10.1159/000206046.
A case of acute leukaemia with t(4;11) chromosomal abnormality in a 28-year-old woman is reported. At diagnosis, two blast cell populations were seen: 60% of the cells were small cells with lymphoid morphology, 40% were large cells with monocytic morphology. Cytochemical examination was consistent with acute myeloid leukaemia (peroxidase-positive in 10% of the cells), but surface markers were those of common acute lymphoblastic leukaemia (CALLA, B4, TdT-positive, but My7-, My9- and OKM1-negative). Five days after diagnosis, although the only treatment had been platelet transfusions, there was a change in morphological and immunological phenotype: 40% of the cells were lymphoid and 60% monocytic. Lymphoid markers were expressed in only 20-40% of cells, and myeloid markers appeared on up to 60% of cells. We conclude that t(4;11) leukaemia could originate in an undifferentiated progenitor cell, which can undergo further differentiation into lymphoblasts or monoblasts, and that we were able to observe this in vivo differentiation in our patient.
报告了一名28岁女性患t(4;11)染色体异常的急性白血病病例。诊断时可见两种原始细胞群:60%的细胞为具有淋巴细胞形态的小细胞,40%为具有单核细胞形态的大细胞。细胞化学检查结果符合急性髓细胞白血病(10%的细胞过氧化物酶阳性),但表面标志物显示为普通急性淋巴细胞白血病(CALLA、B4、TdT阳性,但My7-、My9-和OKM1阴性)。诊断后五天,尽管仅进行了血小板输注治疗,但形态学和免疫表型发生了变化:40%的细胞为淋巴细胞,60%为单核细胞。仅20%-40%的细胞表达淋巴细胞标志物,高达60%的细胞出现髓细胞标志物。我们得出结论,t(4;11)白血病可能起源于未分化的祖细胞,该祖细胞可进一步分化为淋巴母细胞或单核母细胞,并且我们能够在我们的患者中观察到这种体内分化。