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氟达拉滨治疗后低度B细胞淋巴瘤转化中爱泼斯坦-巴尔病毒的检测

Detection of Epstein-Barr virus in transformations of low-grade B-cell lymphomas after fludarabine treatment.

作者信息

Shields D J, Byrd J C, Abbondanzo S L, Lichy J H, Diehl L F, Aguilera N I

机构信息

Department of Pathology, Walter Reed Army Medical Center, Washington, D.C., USA.

出版信息

Mod Pathol. 1997 Nov;10(11):1151-9.

PMID:9388067
Abstract

Fludarabine is a highly effective chemotherapeutic agent for chronic lymphocytic leukemia/small lymphocytic lymphoma and is also active in other B-cell lymphoproliferative disorders. Although highly efficacious in destroying the malignant B-cells, fludarabine also causes T-cell lymphopenia and immunosuppression. We present five patients given fludarabine for low-grade B-cell lymphoproliferative disorders who showed transformation of the primary neoplasm to a higher grade tumor. Immunohistologic antibody studies were performed on paraffin-embedded tissue sections of the initial tissue (when available) and on the follow-up biopsy specimens for CD20, CD3, CD45RO, CD43, CD30, CD15, and latent membrane protein (LMP-1) for Epstein-Barr virus (EBV). The initial diagnoses in these five patients included chronic lymphocytic leukemia/small lymphocytic lymphoma (three cases), follicle center lymphoma (one case), and Waldenstrom's macroglobulinemia (one case). All of the follow-up biopsy specimens showed scattered Hodgkin's-like cells, and two of the five also showed foci of large-cell transformation. The Hodgkin's-like cells showed CD30 immunoreactivity in four of the five cases and CD15 immunoreactivity in three of the five. Strong immunoreactivity of the large, atypical, Hodgkin's-like cells for LMP-1 of EBV was noted in four cases; in the remaining case, this finding was equivocal. In situ hybridization for EBV-encoded RNA was positive in four of the five cases. Molecular studies by polymerase chain reaction (PCR) showed the presence of EBV in three of the five cases. PCR for detection of immunoglobulin heavy chain demonstrated identical monoclonal rearrangements in the original lymphoma and transformation in one case with available material. The CD4 lymphocyte count in each patient was less than 550/microL, indicating cellular dysfunction. Transformation of low-grade non-Hodgkin's lymphomas after fludarabine therapy might be associated with EBV and severe immunosuppression.

摘要

氟达拉滨是治疗慢性淋巴细胞白血病/小淋巴细胞淋巴瘤的一种高效化疗药物,对其他B细胞淋巴增殖性疾病也有活性。尽管氟达拉滨在破坏恶性B细胞方面非常有效,但它也会导致T细胞淋巴细胞减少和免疫抑制。我们报告了5例接受氟达拉滨治疗低度B细胞淋巴增殖性疾病的患者,这些患者的原发性肿瘤转变为高级别肿瘤。对初始组织(如有)的石蜡包埋组织切片以及后续活检标本进行免疫组织化学抗体研究,检测CD20、CD3、CD45RO、CD43、CD30、CD15和爱泼斯坦-巴尔病毒(EBV)的潜伏膜蛋白(LMP-1)。这5例患者的初始诊断包括慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(3例)、滤泡中心淋巴瘤(1例)和华氏巨球蛋白血症(1例)。所有后续活检标本均显示散在的霍奇金样细胞,5例中有2例还显示大细胞转化灶。霍奇金样细胞在5例中有4例显示CD30免疫反应性,5例中有3例显示CD15免疫反应性。4例大的非典型霍奇金样细胞对EBV的LMP-1有强免疫反应性;在其余1例中,这一发现不明确。5例中有4例EBV编码RNA原位杂交呈阳性。聚合酶链反应(PCR)分子研究显示5例中有3例存在EBV。检测免疫球蛋白重链的PCR显示,在1例有可用材料的病例中,原始淋巴瘤和转化灶中有相同的单克隆重排。每位患者的CD4淋巴细胞计数均低于550/μL,表明细胞功能障碍。氟达拉滨治疗后低度非霍奇金淋巴瘤的转化可能与EBV和严重免疫抑制有关。

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