Greenberg B R, Miller C, Cardiff R D, MacKenzie M R, Walling P
Br J Haematol. 1983 Jan;53(1):125-33. doi: 10.1111/j.1365-2141.1983.tb01994.x.
A patient is described who presented with a combined preleukaemic, lymphoproliferative and plasma cell disorder. These disorders were not related to cytotoxic therapy. The clonal nature of the lymphoid component was demonstrated by lymphocyte surface marker studies and the clonal nature of the plasma cell component by immunoperoxidase studies. Since the involved lymphoid and plasma cells contained different heavy and light chains, they were felt to originate from two separate B cell clones not related to the clone responsible for the preleukaemic component.
本文描述了一名患有白血病前期、淋巴细胞增殖性和浆细胞紊乱合并症的患者。这些紊乱与细胞毒性疗法无关。通过淋巴细胞表面标志物研究证实了淋巴样成分的克隆性质,通过免疫过氧化物酶研究证实了浆细胞成分的克隆性质。由于受累的淋巴细胞和浆细胞含有不同的重链和轻链,因此认为它们源自两个独立的B细胞克隆,与导致白血病前期成分的克隆无关。