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EBV may be expressed in the LP cells of nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) in both children and adults

机译:EBV可能在儿童和成人的结节性淋巴细胞为主的霍奇金淋巴瘤(NLPHL)的LP细胞中表达

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摘要

Nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) and classical Hodgkin lymphoma (CHL) are classified separately because of their distinct clinical and pathological features. While EBV is detected in the neoplastic cells of 25-70% of CHL, NLPHL is generally considered to be EBV-negative. We assessed EBV status in 302 pediatric and adult cases of NLPHL. A total of 145 pediatric (age ≤18) and 157 adult cases of NLPHL were retrieved from 3 North American centers and tested for EBV by in situ hybridization (EBER). Clinical and pathological features were analyzed. Five (3.4%) pediatric and 7 (4.5%) adult NLPHL cases contained EBV-positive LP cells. While all 12 cases met criteria for the diagnosis of NLPHL, atypical features were present, including capsular fibrosis, atrophic germinal centers and pleomorphic or atypical lymphocyte predominant (LP) cells. Both CD20 and OCT-2 expression were strong and diffuse in all except one case. However, PAX5 and CD79a were weak and/or variable in 7/8 and 6/6 cases tested, respectively. EBV-positive cases were more likely to be CD30-positive (75%) than EBV-negative cases (25%) (p=0.0007); CD15 was negative in all cases. Our results show that EBV-positive LP cells may occur in NLPHL. Distinguishing EBV+ NLPHL from CHL can be challenging, since EBV+ NLPHL can have partial expression of CD30 and weak PAX5 staining as well as pleomorphic-appearing LP cells. However, the overall appearance and maintenance of B-cell phenotype, with strong and diffuse CD20 and OCT-2 expression, support the diagnosis of NLPHL in these cases.
机译:结节性淋巴细胞优势霍奇金淋巴瘤(NLPHL)和经典霍奇金淋巴瘤(CHL)由于其独特的临床和病理学特征而被分别分类。虽然在CHL的25-70%的肿瘤细胞中检测到EBV,但NLPHL通常被认为是EBV阴性。我们评估了302例小儿和成人NLPHL的EBV状况。从北美的三个中心共检索了145例儿科(≤18岁)和157例成年NLPHL病例,并通过原位杂交(EBER)测试了EBV。临床和病理特征进行了分析。 5例(3.4%)小儿和7例(4.5%)成人NLPHL病例包含EBV阳性LP细胞。尽管所有12例病例均符合NLPHL的诊断标准,但仍存在非典型特征,包括荚膜纤维化,萎缩生发中心和多形性或非典型性淋巴细胞优势(LP)细胞。除一种情况外,CD20和OCT-2的表达均强而弥漫。然而,分别在7/8和6/6的情况下,PAX5和CD79a较弱和/或可变。与EBV阴性病例(25%)相比,EBV阳性病例更有可能是CD30阳性(75%)(p = 0.0007);在所有情况下,CD15均为阴性。我们的结果表明,NLPHL中可能出现EBV阳性LP细胞。从CHL区分EBV + NLPHL可能具有挑战性,因为EBV + NLPHL可能具有CD30的部分表达和弱的PAX5染色以及多形性LP细胞。但是,B细胞表型的整体出现和维持,以及CD20和OCT-2的强表达和弥散表达,在这些情况下都支持NLPHL的诊断。

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