Mahadevan Anita, Rao Clementina Rama, Shanmugham M, Shankar Susarla Krishna
Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.
Department of Pathology, Kidwai Memorial Institute of Oncology, Bangalore, Karnataka, India.
J Neurosci Rural Pract. 2015 Jan;6(1):8-14. doi: 10.4103/0976-3147.143171.
Primary central nervous system diffuse large B-cell lymphoma (PCNSL DLBCL) in the immunocompetent is an uncommon tumor that has an activated B-cell immunophenotype resembling germinal center exit B cells. They also differ from primary central nervous diffuse large B-cell lymphomas in the immunocompromised as they show no association with the Epstein-Barr virus.
To determine if immunophenotypic subtyping of PCNS DLBCL from Asian subcontinent are also different similar to its systemic counterpart is unclear, as there are only limited studies from Asia, and none from India.
The immunohistochemical profile of 24 South Indian patients with primary central nervous system diffuse large B-cell lymphoma was studied using germinal center markers - CD10 and Bcl-6, and activation markers - MUM1 and CD138, which are markers for late/post germinal centre B cells. Insitu hybridization for EBV genome and LMP1 by immunohistochemistry was carried out in all cases to determine association with EBV.
Centroblastic morphology and uniform activated B-cell phenotype with positivity for MUM1 was seen in 91.6% of tumors. Co-expression of Bcl-6 and MUM1 was evident in 50%, which is more frequent than in systemic diffuse large B-cell lymphomas. All cases were negative for Epstein-Barr virus using EBER in-situ hybridization and LMP1 immunohistochemistry.
Primary diffuse large B-cell lymphoma in the immunocompetent is a distinct clinicopathological entity with centroblastic morphology, a uniform activated B-cell immunophenotype that is not associated with the Epstein-Barr virus regardless of geographic origin.
免疫功能正常者的原发性中枢神经系统弥漫性大B细胞淋巴瘤(PCNSL DLBCL)是一种罕见肿瘤,具有类似于生发中心迁出B细胞的活化B细胞免疫表型。它们也与免疫功能低下者的原发性中枢神经系统弥漫性大B细胞淋巴瘤不同,因为它们与爱泼斯坦-巴尔病毒无关联。
由于亚洲仅有有限的研究,而印度尚无相关研究,因此尚不清楚来自亚洲次大陆的PCNS DLBCL的免疫表型亚型是否也与全身对应物不同。
使用生发中心标志物——CD10和Bcl-6,以及活化标志物——MUM1和CD138(晚期/生发中心后B细胞的标志物),研究了24例南印度原发性中枢神经系统弥漫性大B细胞淋巴瘤患者的免疫组化特征。对所有病例进行了EBV基因组原位杂交和LMP1免疫组化检测,以确定与EBV的关联。
91.6%的肿瘤可见中心母细胞形态和MUM1阳性的均匀活化B细胞表型。50%的病例中Bcl-6和MUM1共表达明显,这比全身弥漫性大B细胞淋巴瘤更常见。使用EBER原位杂交和LMP1免疫组化检测,所有病例的爱泼斯坦-巴尔病毒均为阴性。
免疫功能正常者的原发性弥漫性大B细胞淋巴瘤是一种独特的临床病理实体,具有中心母细胞形态、均匀的活化B细胞免疫表型,且无论地理来源如何均与爱泼斯坦-巴尔病毒无关联。