Posttransplant Lymphoproliferative Disorder of the Central Nervous System

被引:28
|
作者
Kempf, Christian [1 ]
Tinguely, Marianne [2 ,3 ]
Rushing, Elisabeth J. [1 ]
机构
[1] Univ Zurich Hosp, Inst Neuropathol, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Inst Surg Pathol, CH-8091 Zurich, Switzerland
[3] Kempf & Pfaltz, Histol Diagnost, Zurich, Switzerland
关键词
Posttransplant lymphoproliferative disorder; Central nervous system; Immunosuppressive therapy; EPSTEIN-BARR-VIRUS; SOLID-ORGAN TRANSPLANTATION; MEMBRANE-PROTEIN; B-CELL LYMPHOMA; C-MYC; LATENT; GENE; EXPRESSION; RECIPIENTS; INFECTION;
D O I
10.1159/000347225
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Posttransplant lymphoproliferative disorder (PTLD) involves uncommon, severe complications following the transplantation of solid organs, bone marrow and stem cells. Despite comprising mainly lymphoid proliferations that are predominantly driven by lymphotropic Epstein-Barr virus (EBV) infections, PTLD often displays substantial morphologic heterogeneity that can pose diagnostic challenges. With the steady increase in transplantations accompanied by potent immunosuppressive therapy, it is important to heighten awareness of this entity among clinicians and pathologists. In comparison to systemic PTLD, cases that primarily manifest in the central nervous system (CNS) are reported to be more severe and to exhibit unique characteristics. So far, only isolated cases and small series have been reported describing CNS involvement in PTLD. In this article, we review the current knowledge, focusing on the histopathological features of primary CNS lymphoproliferative disorders following organ transplantation. copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:310 / 318
页数:9
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