Catovsky D, Goldman J M, Okos A, Frisch B, Galton D A
Br Med J. 1974 Jun 22;2(5920):643-6. doi: 10.1136/bmj.2.5920.643.
Two cases of acute lymphoblastic leukaemia (A.L.L.) of T-cell type are reported. Clinically they were characterized by very high peripheral blood blast cell counts at presentation, the early development of meningeal leukaemia, and relative resistance to treatment with combination chemotherapy. Leukaemic cells from both patients lacked all the B-cell markers investigated, but 60-65% of their cells formed rosettes with sheep red cells. Cytochemical and surface structure studies helped to define additional features of these cells and confirmed their T-cell nature.It seems that this variant of A.L.L. may not be uncommon and that it can be distinguished on clinical and immunological grounds from the usual type of A.L.L. which runs a less aggressive course and lacks B- or T-cell markers.
报告了2例T细胞型急性淋巴细胞白血病(A.L.L.)。临床上,其特征为就诊时外周血原始细胞计数极高、早期发生脑膜白血病以及对联合化疗相对耐药。两名患者的白血病细胞缺乏所检测的所有B细胞标志物,但60% - 65%的细胞与绵羊红细胞形成玫瑰花结。细胞化学和表面结构研究有助于明确这些细胞的其他特征,并证实了它们的T细胞性质。看来这种A.L.L.变体可能并不罕见,并且可以根据临床和免疫学依据与通常病程较缓和且缺乏B或T细胞标志物的A.L.L.类型相区分。