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老年 EBV 阳性弥漫性大 B 细胞淋巴瘤。

Epstein-Barr virus-positive diffuse large B-cell lymphomas of the elderly.

机构信息

Institute of Pathology, Eberhard-Karls-University of Tuebingen, Germany.

出版信息

Adv Anat Pathol. 2011 Sep;18(5):349-55. doi: 10.1097/PAP.0b013e318229bf08.

Abstract

Epstein-Barr virus (EBV)-positive diffuse large B-cell lymphoma (DLBCL) of the elderly has been included in the 2008 WHO classification as a new provisional entity and is defined as blastic, clonal B-cell proliferation associated with EBV occurring in patients over 50 years of age, presumably due to senescence of the immune system. Secondary immunodeficiencies must be excluded. Morphologically, the predominant polymorphic subtype shows a mixed proliferation of large transformed cells, plasma cells, plasmablasts, lymphocytes, and commonly Reed-Sternberg (RS)-like cells, whereas the monomorphic subtype reveals sheets of large cells. An additional characteristic feature is large areas of "geographical" necrosis. EBV+ DLBCL of the elderly is positive for pan-B cell markers and often for CD30. EBV infection detected by Epstein Barr early RNA in situ hybridization should be present in the majority of tumor cells. Most cases express LMP1 and up to 32% EBNA2, the latter a sign of an impaired immune system. The most challenging differential diagnosis is EBV+ classical Hodgkin lymphoma in older patients. Strong, homogeneous expression of B-cell markers, including transcription factors OCT2 and BOB.1, and lack of CD15 support a diagnosis of EBV+ DLBCL. EBV+ DLBCL of the elderly accounts for 8% to 10% of DLBCL in Asian countries, but seems to be uncommon in Western populations, indicating an ethnic or geographic predisposition. Clinically, patients may present with nodal or extranodal involvement. B-symptoms and poor performance status are common, and prognosis is significantly inferior compared with EBV- cases. Whether EBV+DLBCL of the elderly represents a true entity or only a DLBCL variant remains to be determined.

摘要

老年人 EBV 阳性弥漫性大 B 细胞淋巴瘤(DLBCL)已被纳入 2008 年世界卫生组织分类中的一个新的暂定实体,其定义为发生于 50 岁以上患者的与 EBV 相关的、伴有免疫衰老的克隆性 blastoid B 细胞增殖。必须排除继发性免疫缺陷。从形态学上看,主要的多形亚型表现为大转化细胞、浆细胞、浆母细胞、淋巴细胞的混合增殖,通常伴有 Reed-Sternberg(RS)样细胞,而单形亚型则显示大片的大细胞。另一个特征是大片的“地理性”坏死。老年人 EBV+DLBCL 阳性表达 pan-B 细胞标志物,通常还阳性表达 CD30。通过 Epstein-Barr 早期 RNA 原位杂交检测到的 EBV 感染应存在于大多数肿瘤细胞中。大多数病例表达 LMP1 和高达 32%的 EBNA2,后者是免疫系统受损的标志。最具挑战性的鉴别诊断是老年 EBV+经典霍奇金淋巴瘤。强烈、均匀表达 B 细胞标志物,包括转录因子 OCT2 和 BOB.1,以及缺乏 CD15,支持 EBV+DLBCL 的诊断。老年人 EBV+DLBCL 占亚洲国家 DLBCL 的 8%至 10%,但在西方人群中似乎不常见,表明存在种族或地理倾向。临床上,患者可能表现为淋巴结或结外受累。B 症状和较差的表现状态很常见,与 EBV-病例相比,预后明显较差。老年人 EBV+DLBCL 是否代表真正的实体或只是一种 DLBCL 变体仍有待确定。

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