Sun T, Susin M, Brody J, Dittmar K, Teichberg S, Weiner R, Lin J H, Felber N
Department of Laboratories, North Shore University Hospital-Cornell University Medical College, Manhasset, NY 11030.
Am J Hematol. 1994 Jan;45(1):39-50. doi: 10.1002/ajh.2830450107.
Splenic lymphoma with villous lymphocytes (SLVL) is a relatively new entity with only a few reports published. We report seven cases of SLVL with detailed clinicopathologic and comprehensive immunophenotypic studies to further characterize this lymphoma, which is frequently confused with hairy cell leukemia and other low-grade B-cell lymphoid neoplasms. The diagnostic criteria we used include 1) prominent splenomegaly, 2) insignificant or no lymphadenopathy, 3) lymphocytosis without leukopenia, 4) presence of circulating villous lymphocytes, 5) characteristic cytologic and histologic features, and 6) specific phenotypic and cytochemical findings. Our studies show that SLVL does not represent a pure entity but rather a morphologically heterogeneous group of low-grade lymphomas with various cytologic and histologic features. Although immunophenotyping is helpful in differential diagnosis, multiparameter studies are necessary to confirm the diagnosis. In our series, only two patients died of SLVL, who probably developed transformation to a higher-grade lymphoma.
伴有绒毛状淋巴细胞的脾淋巴瘤(SLVL)是一种相对较新的疾病实体,仅有少数相关报道发表。我们报告7例伴有绒毛状淋巴细胞的脾淋巴瘤患者,并对其进行详细的临床病理及全面的免疫表型研究,以进一步明确这种常与毛细胞白血病及其他低度B细胞淋巴瘤相混淆的淋巴瘤的特征。我们采用的诊断标准包括:1)显著脾肿大;2)无或仅有轻微淋巴结肿大;3)淋巴细胞增多且无白细胞减少;4)存在循环绒毛状淋巴细胞;5)特征性的细胞学和组织学特征;6)特异性的表型和细胞化学表现。我们的研究表明,伴有绒毛状淋巴细胞的脾淋巴瘤并非一个单纯的疾病实体,而是一组形态学上异质性的低度淋巴瘤,具有多种细胞学和组织学特征。尽管免疫表型分析有助于鉴别诊断,但多参数研究对于确诊是必要的。在我们的病例系列中,仅有2例患者死于伴有绒毛状淋巴细胞的脾淋巴瘤,他们可能发生了向高级别淋巴瘤的转化。