Miyazaki Mutsuko, Taguchi Akihiko, Sakuragi Shizu, Mitani Noriyuki, Matsuda Kazuyuki, Shinohara Kenji
Division of Hematology, Department of Medicine, Yamaguchi Prefecture Central Hospital.
Rinsho Ketsueki. 2004 May;45(5):405-7.
A 67-year-old male was admitted because of lymphocytosis and huge splenomegaly. Abnormal lymphocytes had cytoplasmic hairy projections and were negative for tartrate-resistant acid phosphatase staining. The bone marrow aspirate contained many lymphocytes with the same morphology. Flow cytometric analysis revealed an increase in IgM and kappa positive B cells. They were positive for CD11c, CD19, CD20 and FMC7, and negative for CD5, CD10 and CD25. The patient was diagnosed as having hairy cell leukemia, Japanese variant. Initially interferon-alpha was administered for a month, decreasing the numbers of leukemic cells but with little effect on splenomegaly. Subsequent administration of cladribine (0.09 mg/kg, 7 days) showed a remarkable effect, and the patient has been in complete remission for 8 months.
一名67岁男性因淋巴细胞增多和巨脾症入院。异常淋巴细胞有细胞质毛状突起,抗酒石酸酸性磷酸酶染色呈阴性。骨髓穿刺液中有许多形态相同的淋巴细胞。流式细胞术分析显示IgM和κ阳性B细胞增多。它们CD11c、CD19、CD20和FMC7呈阳性,CD5、CD10和CD25呈阴性。该患者被诊断为日本变异型毛细胞白血病。最初给予α干扰素治疗一个月,白血病细胞数量减少,但对脾肿大几乎没有影响。随后给予克拉屈滨(0.09mg/kg,7天)显示出显著效果,患者已完全缓解8个月。