Jabłońska Joanna, Jesionek-Kupnicka Dorota
Department of Pathology, Medical University of Łodź.
Pol J Pathol. 2008;59(3):121-7.
Although diffuse large B cell lymphomas (DLBCL) are considered in the WHO classification a specific histopathological type, their diversity in the clinical features, morphology and molecular aberrations strongly suggest that these tumors represent a heterogeneous group of neoplasms rather than a single clinicopathological entity. There have been various approaches to differentiate between separate nosological entities within DLBCLs based on various methods, such as the microarray technique or immunohistochemistry. Although it has been proven that gene expression profiling using cDNA microarrays could identify prognostically important subgroup of DLBCL: germinal center B-cell (GCB)-like DLBCL and activated B-cell (ABC)-like DLBCL, this method is impractical as a clinical tool. Therefore, investigators have started using immunohistochemistry in their studies. Employing various immunohistochemical antibodies, such as CD10, CD138, anti-Bcl-2, anti-Bcl-6, MUM1 and anti-p53, several groups have aimed at subclassifying DLBCL into the GCB and ABC subgroups with comparable differences in clinical behavior. This review summarizes these data and indicates their impact on DLBCL classification.
尽管弥漫性大B细胞淋巴瘤(DLBCL)在世界卫生组织分类中被视为一种特定的组织病理学类型,但它们在临床特征、形态学和分子异常方面的多样性强烈表明,这些肿瘤代表的是一组异质性肿瘤,而非单一的临床病理实体。基于多种方法,如微阵列技术或免疫组织化学,已经有各种方法来区分DLBCL内不同的疾病分类实体。尽管已证明使用cDNA微阵列进行基因表达谱分析可以识别出具有预后重要性的DLBCL亚组:生发中心B细胞(GCB)样DLBCL和活化B细胞(ABC)样DLBCL,但该方法作为一种临床工具并不实用。因此,研究人员已开始在其研究中使用免疫组织化学。通过使用各种免疫组织化学抗体,如CD10、CD138、抗Bcl-2、抗Bcl-6、MUM1和抗p53,几个研究小组旨在将DLBCL细分为GCB和ABC亚组,它们在临床行为上存在类似差异。本综述总结了这些数据,并指出了它们对DLBCL分类的影响。