Moore Erika M, Swerdlow Steven H, Gibson Sarah E
University of Pittsburgh School of Medicine, Pittsburgh, PA 15213.
University of Pittsburgh School of Medicine, Pittsburgh, PA 15213.
Hum Pathol. 2017 Oct;68:47-53. doi: 10.1016/j.humpath.2017.08.015. Epub 2017 Aug 26.
Although most classical Hodgkin lymphomas (CHLs) are easily distinguished from nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) and primary mediastinal large B-cell lymphoma (PMBL), cases with significant CD20 expression cause diagnostic confusion. Although the absence of OCT-2 and BOB.1 are useful in these circumstances, a variable proportion of CHLs are positive for these antigens. We investigated the utility of J chain and myocyte enhancer factor 2B (MEF2B) in the diagnosis of CHL; NLPHL; PMBL; T-cell/histiocyte-rich large B-cell lymphoma (TCRLBL); and B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and CHL, compared with OCT-2 and BOB.1. J chain and MEF2B highlighted lymphocyte predominant (LP) cells in 20/20 (100%) NLPHLs and were negative in 43/43 (100%) CHLs. Fourteen of 15 (93%) PMBLs and 4/4 (100%) TCRLBLs were MEF2B positive, whereas 67% of PMBLs and 50% of TCRLBLs were J chain positive. Three of 3 B-cell lymphomas, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and CHL, were negative for J chain and MEF2B. J chain and MEF2B were 100% sensitive and specific for NLPHL versus CHL. MEF2B was 100% sensitive and 98% specific for PMBL versus CHL. Whereas loss of OCT-2 and/or BOB.1 expression had a sensitivity of only 86% and specificity of 100% for CHL versus NLPHL, PMBL, and TCRLBL, lack of both J chain and MEF2B expression was 100% sensitive and 97% specific. J chain and MEF2B are highly sensitive and specific markers of NLPHL versus CHL; are particularly useful in highlighting LP cells; and, with rare exception, are of greater utility than OCT-2 and BOB.1 in differentiating CHL from NLPHL and other large B-cell lymphomas.
尽管大多数经典型霍奇金淋巴瘤(CHL)很容易与结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)和原发性纵隔大B细胞淋巴瘤(PMBL)区分开来,但CD20表达显著的病例会导致诊断混淆。尽管在这些情况下OCT-2和BOB.1的缺失很有用,但仍有可变比例的CHL对这些抗原呈阳性。我们研究了J链和肌细胞增强因子2B(MEF2B)在CHL、NLPHL、PMBL、富于T细胞/组织细胞的大B细胞淋巴瘤(TCRLBL)以及具有弥漫性大B细胞淋巴瘤和CHL之间中间特征的不可分类B细胞淋巴瘤诊断中的效用,并与OCT-2和BOB.1进行了比较。J链和MEF2B在20/20(100%)的NLPHL中突出显示淋巴细胞为主型(LP)细胞,而在43/43(100%)的CHL中呈阴性。15例PMBL中有14例(93%)和4例TCRLBL均为MEF2B阳性,而67%的PMBL和50%的TCRLBL为J链阳性。3例具有弥漫性大B细胞淋巴瘤和CHL之间中间特征的不可分类B细胞淋巴瘤均为J链和MEF2B阴性。J链和MEF2B对NLPHL与CHL的敏感性和特异性均为100%。MEF2B对PMBL与CHL的敏感性为100%,特异性为98%。而OCT-2和/或BOB.1表达缺失对CHL与NLPHL、PMBL和TCRLBL的敏感性仅为86%,特异性为100%,J链和MEF2B表达均缺失的敏感性为100%,特异性为97%。J链和MEF2B是NLPHL与CHL的高度敏感和特异性标志物;在突出显示LP细胞方面特别有用;并且,除极少数例外,在区分CHL与NLPHL及其他大B细胞淋巴瘤方面比OCT-2和BOB.1更有用。