Salama Mohamed E, Lossos Izidore S, Warnke Roger A, Natkunam Yasodha
Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Am J Clin Pathol. 2009 Jul;132(1):39-49. doi: 10.1309/AJCPZQ1GXBBNG8OG.
Nodal marginal zone lymphoma (NMZL) represents a rare and heterogeneous group that lacks markers specific for the diagnosis. We evaluated morphologic and immunoarchitectural features of 51 NMZLs, and the following immunostains were performed: CD20, CD21, CD23, CD5, CD3, CD43, CD10, Ki-67, BCL1, BCL2, BCL6, HGAL, and LMO2. Four immunoarchitectural patterns were evident: diffuse (38 [75%]), well-formed nodular/follicular (5 [10%]), interfollicular (7 [14%]), and perifollicular (1 [2%]). Additional features included a monocytoid component (36 [71%]), admixed large cells (20 [39%]), plasma cells (24 [47%]), compartmentalizing stromal sclerosis (13 [25%]), and prominent blood vessel sclerosis (10 [20%]). CD21 highlighted disrupted follicular dendritic cell meshwork in 35 (71%) of 49 cases, and CD43 coexpression was present in 10 (24%) of 42 cases. A panel of germinal center-associated markers was helpful in eliminating cases of diffuse follicle center lymphoma. Our results highlight the histologic and immunoarchitectural spectrum of NMZL and the usefulness of immunohistochemical analysis for CD43, CD23, CD21, BCL6, HGAL, and LMO2 in the diagnosis of NMZL.
结外边缘区淋巴瘤(NMZL)是一组罕见且异质性的疾病,缺乏特异性诊断标志物。我们评估了51例NMZL的形态学和免疫结构特征,并进行了以下免疫染色:CD20、CD21、CD23、CD5、CD3、CD43、CD10、Ki-67、BCL1、BCL2、BCL6、HGAL和LMO2。明显呈现出四种免疫结构模式:弥漫性(38例[75%])、形成良好的结节/滤泡性(5例[10%])、滤泡间(7例[14%])和滤泡周围(1例[2%])。其他特征包括单核细胞样成分(36例[71%])、混合大细胞(20例[39%])、浆细胞(24例[47%])、分隔性间质硬化(13例[25%])和显著的血管硬化(10例[20%])。49例中的35例(71%)CD21显示滤泡树突状细胞网络破坏,42例中的10例(24%)存在CD43共表达。一组生发中心相关标志物有助于排除弥漫性滤泡中心淋巴瘤病例。我们的结果突出了NMZL的组织学和免疫结构谱,以及免疫组化分析CD43、CD23、CD21、BCL6、HGAL和LMO2在NMZL诊断中的实用性。