Ho C H, Chiang Y M, Chong L L, Lin H Y, Hwang T S
Scand J Haematol. 1985 Aug;35(2):246-8. doi: 10.1111/j.1600-0609.1985.tb01582.x.
Persistent lymphocytosis and intermittent fever were found in a 68-yr-old Chinese woman 5 yr after the diagnosis of Sjögren's syndrome with systemic lupus erythematosus (SLE). A series of examinations--including virology, bone marrow aspiration and surface markers of lymphocytes--was made to evaluate the nature of the lymphocytosis which had not been found previously. All of the results were consistent with the diagnosis of B-cell chronic lymphocytic leukaemia (CLL). Development of CLL in Sjögren's syndrome has seldom been described before and may be added to other malignancies associated with Sjögren's syndrome.
一名68岁的中国女性在被诊断为干燥综合征合并系统性红斑狼疮(SLE)5年后,出现了持续性淋巴细胞增多和间歇性发热。进行了一系列检查,包括病毒学检查、骨髓穿刺和淋巴细胞表面标志物检查,以评估此前未发现的淋巴细胞增多的性质。所有结果均符合B细胞慢性淋巴细胞白血病(CLL)的诊断。干燥综合征患者发生CLL此前鲜有报道,可能会被纳入与干燥综合征相关的其他恶性肿瘤之列。