Richard J L, Vives J F, Clot J, Taib J, Lambert M F, Janbon C, Vallat G
Sem Hop. 1981;57(29-32):1333-7.
Prolymphocytic leukaemia (PL) is a rare variant of lympho-proliferative disorder, defined by Galton [21], which differs clearly from CLL by clinical, haematological and immunological features. Nevertheless like CLL, PL appears to represent predominantly a B cells monoclonal proliferation and cases of T-PL are rare. We report about another case of PL which was found to have T-lymphocyte characteristics and some clinical and immunological particularities.
幼淋巴细胞白血病(PL)是一种罕见的淋巴细胞增殖性疾病变体,由高尔顿[21]定义,其在临床、血液学和免疫学特征上与慢性淋巴细胞白血病(CLL)明显不同。然而,与CLL一样,PL似乎主要代表B细胞单克隆增殖,而T-PL病例很少见。我们报告了另一例PL病例,该病例被发现具有T淋巴细胞特征以及一些临床和免疫学特殊性。