Yamada T, Ninomiya H, Horiuchi T, Takada K, Hato T, Yamauchi K, Yasukawa M, Fujita S
First Department of Internal Medicine, School of Medicine, Ehime University.
Rinsho Ketsueki. 1995 Oct;36(10):1230-2.
A 39-year-old male was referred to our hospital in June, 1993, because of leukocytosis. Physical examinations showed massive splenomegaly without any lymphadenopathy. The white blood cell count was 13,800/microliters with 87% morphologically mature lymphocytes. Bone marrow aspirate revealed hypercellularity with 67% lymphocytes morphologically similar to peripheral lymphocytes. The lymphocytes displayed monoclonal rearrangements of immunoglobulin genes and the phenotype of CD5-CD19+CD20+ CD21+ and Smlg+. Splenectomy was effective against neutropenia and thromboytopenia. The clinical and laboratory findings of this case were unusual compared to those of typical B-CLL in massive splenomegaly, no lymphadenopathy and CD5-phenotype, suggesting the heterogeneity of B-CLL.
1993年6月,一名39岁男性因白细胞增多症转诊至我院。体格检查显示脾脏肿大明显,无任何淋巴结病。白细胞计数为13,800/微升,其中87%为形态学成熟淋巴细胞。骨髓穿刺显示细胞增多,67%的淋巴细胞在形态上与外周淋巴细胞相似。这些淋巴细胞显示免疫球蛋白基因的单克隆重排,表型为CD5-CD19+CD20+CD21+和Smlg+。脾切除术对中性粒细胞减少症和血小板减少症有效。与典型B细胞慢性淋巴细胞白血病相比,该病例在脾脏肿大明显、无淋巴结病和CD5表型方面的临床和实验室检查结果不寻常,提示B细胞慢性淋巴细胞白血病的异质性。