Cavalli F, Pedrinis E, Ludin J, Goldhirsch A, Tatti V
Dtsch Med Wochenschr. 1977 Oct 14;102(41):1443-5. doi: 10.1055/s-0028-1105517.
A 67-year-old woman, at first diagnosed to have acute lymphocytic leukaemia, developed all the characteristic signs of so-called prolymphocytic leukaemia, namely severe general symptoms of illness, marked hepatosplenomegaly in the absence of lymphadenopathy, extreme leukocytosis (at times more than 1000 x 10(9)/l). Prolymphocytic leukaemia is now considered to be an especially unfavourable form of chronic lymphocytic leukaemia.
一名67岁女性,最初被诊断为急性淋巴细胞白血病,后来出现了所谓原淋巴细胞白血病的所有特征性体征,即严重的全身症状、无淋巴结病情况下显著的肝脾肿大、极度白细胞增多(有时超过1000×10⁹/L)。原淋巴细胞白血病现被认为是慢性淋巴细胞白血病的一种特别不良的形式。