Hsi E D, Picken M M, Alkan S
Department of Pathology, Loyola University Medical Center, Maywood, Illinois, USA.
Mod Pathol. 1998 May;11(5):479-84.
Post-transplantation lymphoproliferative disorders (PTLDs) are primarily B-cell disorders that are thought to be Epstein-Barr virus (EBV) driven and that can occur months to years after solid organ or bone marrow transplantation. A small percentage of cases have also been shown to be T-cell phenotype, but a PTLD of NK-cell type has not been previously described. We report here the case of a renal transplant recipient in whom a clinically aggressive, histologically monomorphic PTLD developed that was documented to be of an NK-cell phenotype according to paraffin section and flow cytometric immunophenotyping. Molecular-genetic analysis showed the PTLD to contain germline immunoglobulin heavy, kappa light chain, and T-cell receptor beta and gamma genes. Studies for EBV failed to demonstrate the presence of viral infection in tumor cells. Clinical follow-up showed a rapidly fatal course. To our knowledge, this is the first reported case of an EBV-negative PTLD of true NK-cell type.
移植后淋巴细胞增生性疾病(PTLD)主要是B细胞疾病,被认为由 Epstein-Barr病毒(EBV)驱动,可在实体器官或骨髓移植数月至数年之后发生。一小部分病例也显示为T细胞表型,但此前尚未描述过NK细胞型PTLD。我们在此报告一例肾移植受者,其发生了临床上具有侵袭性、组织学上为单形性的PTLD,根据石蜡切片和流式细胞术免疫表型分析,该PTLD被证实为NK细胞表型。分子遗传学分析显示,该PTLD含有种系免疫球蛋白重链、κ轻链以及T细胞受体β和γ基因。针对EBV的研究未能证明肿瘤细胞中存在病毒感染。临床随访显示病程迅速致命。据我们所知,这是首例报告的真正NK细胞型EBV阴性PTLD病例。