首页> 外文期刊>Experimental and clinical transplantation >Posttransplant Lymphoproliferative Disease and Inhibitors of Mammalian Target of Rapamycin: When a Quick Look Back Can Change the Perspective
【24h】

Posttransplant Lymphoproliferative Disease and Inhibitors of Mammalian Target of Rapamycin: When a Quick Look Back Can Change the Perspective

机译:移植后的淋巴细胞增生性疾病和雷帕霉素哺乳动物靶标的抑制剂:快速回顾可以改变观点

获取原文
           

摘要

Posttransplant lymphoproliferative disease represents a heterogeneous group of diseases characterized by uncontrolled proliferation of lymphocytes, favored by immunosuppression. Several risk factors for its development have been described, with Epstein-Barr virus infection being a main cause of early-onset forms and chronic antigen stimulation of donors and/or accumulated immunosuppression as key factors of later forms of lymphocyte transformation. The present clinical case presents a patient diagnosed with post-transplant lymphoproliferative disease 3 years after renal transplant who had a potentially lethal complication related to conversion to inhibitors of mammalian target of rapamycin. Because clinical studies that establish the most suitable treatment are lacking, it is recommended to identify the strategy, defining possible risks versus benefits of conversion to inhibitors of mammalian target of rapamycin in cases of posttransplant lympho-proliferative disease, and to maintain a high level of surveillance in case of possible secondary effects that can be verified after their introduction.
机译:移植后淋巴细胞增生性疾病代表了一组异质性疾病,其特征在于淋巴细胞不受控制的增殖,并受到免疫抑制的青睐。已经描述了其发展的几种危险因素,其中爱泼斯坦-巴尔病毒感染是早期发作形式的主要原因,并且是供体的慢性抗原刺激和/或积累的免疫抑制,是后来淋巴细胞转化形式的关键因素。本临床病例介绍了一名在肾移植后3年被诊断患有移植后淋巴组织增生性疾病的患者,该患者具有与转化为雷帕霉素哺乳动物靶标抑制剂有关的潜在致命并发症。由于尚缺乏确定最合适治疗方法的临床研究,因此建议确定策略,确定在移植后淋巴增生性疾病病例中转用雷帕霉素哺乳动物靶标抑制剂的可能风险与获益,并维持较高水平监视可能的次要影响,并在引入后进行验证。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号