Koza I, Babusíková O
Cancer Research Institute of the Slovak Academy of Sciences, Bratislava, Czechoslovakia.
Neoplasma. 1988;35(1):77-80.
A patient with a seven-year history of polycythemia vera treated by repeated phlebotomies and intermittent busulfan administration developed gradually lymphocytosis accompanied by thrombocytopenia in peripheral blood and in the bone marrow. A marked pathological monoclonal proliferation of the B-cell population was detected. The sequential development of chronic lymphocytic leukemia in the patient with polycythemia vera could be considered as a coincidence because there is no reliable explanation of this event at present.
一名真性红细胞增多症病史七年的患者,经反复放血和间歇性使用白消安治疗,外周血和骨髓中逐渐出现淋巴细胞增多并伴有血小板减少。检测到B细胞群体有明显的病理性单克隆增殖。真性红细胞增多症患者继发慢性淋巴细胞白血病可被视为一种巧合,因为目前对此现象尚无可靠的解释。