Hoffman Mark A
Department of Medicine, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Hematol Oncol Clin North Am. 2006 Oct;20(5):1065-73. doi: 10.1016/j.hoc.2006.06.003.
HCL typically presents in middle-aged men, and is characterized by splenomegaly and cytopenias. Hepatomegaly may be present, but it usually is not a salient feature. Peripheral adenopathy is uncommon. Other organ manifestations occur, but are unusual. patients are now presenting with a less tumor burden, as a result of earlier diagnosis. Leukocytosis/lymphocytosis should suggest HCl variant. Infectious complications, which were common in the past and the major cause of death, have become rare in the era of purine analog therapy. Whether there is a true increased risk for second malignancies remains controversial.
毛细胞白血病(HCL)通常发生于中年男性,其特征为脾肿大和血细胞减少。可能会出现肝肿大,但通常不是显著特征。外周淋巴结病并不常见。其他器官表现也会出现,但不常见。由于早期诊断,现在患者的肿瘤负荷较小。白细胞增多/淋巴细胞增多应提示HCL变异型。感染性并发症在过去很常见且是主要死因,在嘌呤类似物治疗时代已变得罕见。是否存在第二原发恶性肿瘤的真正风险增加仍存在争议。