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本研究通过对祖细胞的检测来进一步探索多毛细胞白血病(HCL)全血细胞减少的机理。由于HCL 患者常呈“干抽”,要从骨髓得到祖细胞来研究是困难的。因此,作者试用患者的周围血来检测祖细胞,并且将结果与其他“白血病性”淋巴增殖性疾病作了比较。研究对象:14例 HCL,2例急淋(ALL),3例慢淋(CLL)。其中8例 HCL,2例 ALL,3例 CLL 除支持措施外,未接受过其他治疗.6例HCL 已切除脾脏。15位正常人的周围血用作对照。
In this study, the detection of progenitor cells to further explore the hairy cell leukemia (HCL) pancytopenia mechanism. Because HCL patients are often “dry pumping”, it is difficult to study progenitor cells from the bone marrow. Therefore, the authors test the peripheral blood of patients to detect progenitor cells and compare the results with other “leukemic” lymphoproliferative disorders. Study subjects: 14 cases of HCL, 2 cases of acute lymphoblastic (ALL), 3 cases of CLL. Among them, 8 cases of HCL, 2 cases of ALL and 3 cases of CLL did not receive any other treatment except for the supportive measures, and six cases of HCL had resection of the spleen. Peripheral blood of 15 normal people served as a control.