Nelson B P, Nalesnik M A, Bahler D W, Locker J, Fung J J, Swerdlow S H
Department of Pathology, University of Pittsburgh School of Medicine, PA, USA.
Am J Surg Pathol. 2000 Mar;24(3):375-85. doi: 10.1097/00000478-200003000-00006.
Post-transplant lymphoproliferative disorders (PTLDs) are usually but not invariably associated with Epstein-Barr virus (EBV). The reported incidence, however, of EBV-negative PTLDs varies widely, and it is uncertain whether they should be considered analogous to EBV-positive PTLDs and whether they have any distinctive features. Therefore, the EBV status of 133 PTLDs from 80 patients was determined using EBV-encoded small ribonucleic acid (EBER) in situ hybridization stains with or without Southern blot EBV terminal repeat analysis. The morphologic, immunophenotypic, genotypic, and clinical features of the EBV-negative PTLDs were reviewed, and selected features were compared with EBV-positive cases. Twenty-one percent of patients had at least one EBV-negative PTLD (14% of biopsies). The initial EBV-negative PTLDs occurred a median of 50 months post-transplantation compared with 10 months for EBV-positive cases. Although only 2% of PTLDs from before 1991 were EBV negative, 23% of subsequent PTLDs were EBV negative (p <0.001). Of the EBV-negative PTLDs, 67% were of monomorphic type (M-PTLD) compared with 42% of EBV-positive cases (p <0.05). The other EBV-negative PTLDs were of infectious mononucleosis-like, plasma cell-rich (n = 2), small B-cell lymphoid neoplasm, large granular lymphocyte disorder (n = 4) and polymorphic (P) types. B-cell clonality was established in 14 specimens and T-cell clonality was established in three (two patients). None of the remaining specimens were studied with Southern blot analysis and some had no ancillary studies. Rearrangement of c-MYC was identified in two M-PTLDs with small noncleaved-like features, and rearrangement of BCL-2 was found in one large noncleaved-like M-PTLD. Ten patients were alive at 3 to 63 months (only three patients received chemotherapy). Seven patients, all with M-PTLDs, are dead at 0.3 to 6 months. Therefore, EBV-negative PTLDs have distinct features, but some do respond to decreased immunosuppression, similar to EBV-positive cases, suggesting that EBV positivity should not be an absolute criterion for the diagnosis of a PTLD.
移植后淋巴组织增生性疾病(PTLD)通常但并非总是与爱泼斯坦-巴尔病毒(EBV)相关。然而,EBV阴性PTLD的报告发病率差异很大,尚不确定它们是否应被视为与EBV阳性PTLD类似,以及它们是否有任何独特特征。因此,使用EBV编码的小核糖核酸(EBER)原位杂交染色并结合或不结合Southern印迹EBV末端重复序列分析,确定了80例患者的133例PTLD的EBV状态。回顾了EBV阴性PTLD的形态学、免疫表型、基因型和临床特征,并将选定特征与EBV阳性病例进行了比较。21%的患者至少有1例EBV阴性PTLD(活检标本的14%)。最初的EBV阴性PTLD发生在移植后中位数50个月,而EBV阳性病例为10个月。虽然1991年以前的PTLD中只有2%为EBV阴性,但随后的PTLD中有23%为EBV阴性(p<0.001)。在EBV阴性PTLD中,67%为单形性类型(M-PTLD),而EBV阳性病例为42%(p<0.05)。其他EBV阴性PTLD为传染性单核细胞增多症样、富含浆细胞型(n=2)、小B细胞淋巴瘤、大颗粒淋巴细胞疾病(n=4)和多形性(P)类型。14份标本确定为B细胞克隆性,3份(2例患者)确定为T细胞克隆性。其余标本均未进行Southern印迹分析,部分标本未进行辅助研究。在2例具有小无裂细胞样特征的M-PTLD中鉴定出c-MYC重排,在1例大无裂细胞样M-PTLD中发现BCL-2重排。10例患者在3至63个月时存活(只有3例患者接受了化疗)。7例患者均为M-PTLD,在0.3至6个月时死亡。因此,EBV阴性PTLD具有独特特征,但有些确实对免疫抑制降低有反应,类似于EBV阳性病例,这表明EBV阳性不应作为PTLD诊断的绝对标准。