Nelson Beverly P, Variakojis Daina, Peterson LoAnn C
Section of Hematopathology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Mod Pathol. 2002 Nov;15(11):1111-20. doi: 10.1097/01.MP.0000031710.32235.24.
Six cases of non-Hodgkin B-cell lymphoma that mimicked either chronic lymphocytic leukemia (CLL) or a CLL variant at presentation are reported. The patients ranged from 54 to 89 years and included three females and three males. All six patients had prominent peripheral blood lymphocytosis at presentation; the initial morphologic impression was CLL in three cases, CLL/prolymphocytic leukemia (PLL) in two cases, and PLL in one. Five patients had bone marrow biopsies; each showed a lymphoid infiltrate in a focally random, interstitial, and/or diffuse pattern. Flow cytometric immunophenotyping showed CD20-positive B cells with surface immunoglobulin (Ig) light chain restriction in all six patients. The five cases resembling CLL or CLL/PLL had at least a subset of CD5-positive B cells, whereas CD5 was absent in the one case that resembled PLL. CD23 was positive in three of the four cases studied that resembled CLL or CLL/PLL; CD79b was positive in three, FMC7 was positive in two, and surface Ig and CD20 were brightly positive in three. A t(11;14) (q13;q32) was found in four cases that resembled CLL or CLL/PLL; they were subsequently diagnosed as mantle cell lymphoma. The remaining two cases mimicking CLL or PLL were diagnosed as lymphomas of follicle center origin with leukemic phase based on the presence of t(14;18) (q32;q21). Thus although the morphology of these six cases resembled CLL or variants, and immunophenotyping by flow cytometry showed overlapping features, genetic studies enabled distinction of these leukemic non-Hodgkin lymphoma from chronic lymphocytic leukemia or variants.
报告了6例初诊时酷似慢性淋巴细胞白血病(CLL)或CLL变异型的非霍奇金B细胞淋巴瘤。患者年龄在54至89岁之间,包括3名女性和3名男性。所有6例患者初诊时均有明显的外周血淋巴细胞增多;最初的形态学印象是3例为CLL,2例为CLL/幼淋巴细胞白血病(PLL),1例为PLL。5例患者进行了骨髓活检;每例均显示局灶性随机、间质和/或弥漫性模式的淋巴细胞浸润。流式细胞术免疫表型分析显示,所有6例患者的CD20阳性B细胞均有表面免疫球蛋白(Ig)轻链限制。5例类似CLL或CLL/PLL的病例至少有一部分CD5阳性B细胞,而1例类似PLL的病例中CD5阴性。在4例类似CLL或CLL/PLL的研究病例中,CD23阳性;3例CD79b阳性,2例FMC7阳性,3例表面Ig和CD20强阳性。在4例类似CLL或CLL/PLL的病例中发现了t(11;14) (q13;q32);随后它们被诊断为套细胞淋巴瘤。其余2例类似CLL或PLL的病例根据存在t(14;18) (q32;q21)被诊断为伴有白血病期的滤泡中心源性淋巴瘤。因此,尽管这6例病例的形态学类似CLL或其变异型,且流式细胞术免疫表型分析显示有重叠特征,但基因研究能够将这些白血病性非霍奇金淋巴瘤与慢性淋巴细胞白血病或其变异型区分开来。