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CD5阴性、CD10阴性的小B细胞白血病:慢性淋巴细胞白血病的变异型还是一种独特的疾病实体?

CD5-negative, CD10-negative small B-cell leukemia: variant of chronic lymphocytic leukemia or a distinct entity?

作者信息

Sheikh Salwa S, Kallakury Bhaskar V S, Al-Kuraya Khawla A, Meck Jeanne, Hartmann Dan P, Bagg Adam

机构信息

Pathology Services Division, Saudi Aramco, Dhahran Health Center, Saudi Arabia.

出版信息

Am J Hematol. 2002 Dec;71(4):306-10. doi: 10.1002/ajh.10222.

Abstract

CD5- and CD10-negative chronic lymphocytic leukemias are quite uncommon as compared to the CD5-positive CLL. We reviewed 250 sequential cases of peripheral blood lymphocytosis to characterize cases of small B-cell lymphoproliferative disorders, submitted with a clinical diagnosis of chronic lymphocytic leukemia exhibiting a non-classic immunophenotypic profile. Six cases of CD5-, CD10-negative chronic lymphocytic leukemias and no tissue involvement were identified that revealed high-density surface-membrane immunoglobulin and CD20 expression, with variable expression of CD11c, CD23, and CD25. Most had a profound leukocytosis (mean WBC 180 x 10(9)/L) with proliferation of mature-appearing lymphocytes. Subsequent bone marrow biopsies showed diffuse infiltration by neoplastic cells in all evaluated patients. The clinical course appeared indolent, with follow-up revealing three patients alive (survival time 38-68 months), while two died of unrelated causes and one was lost to follow-up soon after diagnosis. These cases may represent somewhat unusual chronic lymphoproliferative disorders, with morphologic features and immunophenotypic profile not readily classifiable, but which are certainly atypical for classic chronic lymphocytic leukemia. Some of these features are reminiscent of those seen in marginal-zone lymphoma. However, it is most unusual for this known to be tissue-based disease to present primarily as leukemia rather than lymphoma.

摘要

与CD5阳性的慢性淋巴细胞白血病相比,CD5和CD10阴性的慢性淋巴细胞白血病相当少见。我们回顾了250例连续性外周血淋巴细胞增多症病例,以对小B细胞淋巴增殖性疾病病例进行特征描述,这些病例临床诊断为慢性淋巴细胞白血病,表现出非经典免疫表型特征。我们识别出6例CD5和CD10阴性、无组织受累的慢性淋巴细胞白血病,这些病例显示高密度表面膜免疫球蛋白和CD20表达,CD11c、CD23和CD25表达各异。多数病例有显著的白细胞增多(平均白细胞计数180×10⁹/L),伴有成熟外观淋巴细胞的增殖。随后的骨髓活检显示,所有接受评估的患者均有肿瘤细胞的弥漫浸润。临床病程呈惰性,随访发现3例患者存活(生存时间38 - 68个月),2例死于无关原因,1例在诊断后不久失访。这些病例可能代表一些不寻常的慢性淋巴增殖性疾病,其形态学特征和免疫表型特征不易分类,但肯定不符合经典慢性淋巴细胞白血病的特征。其中一些特征让人联想到边缘区淋巴瘤所见的特征。然而,这种已知为基于组织的疾病主要表现为白血病而非淋巴瘤是非常不寻常的。

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