Abbas Fedaey, El Kossi Mohsen, Shaheen Ihab Sakr, Sharma Ajay, Halawa Ahmed
Nephrology Department, Jaber El Ahmed Military Hospital, Safat 13005, Kuwait.
Faculty of Health and Science, University of Liverpool, Institute of Learning and Teaching, School of Medicine, Liverpool L69 3GB, United Kingdom.
World J Transplant. 2020 Feb 28;10(2):29-46. doi: 10.5500/wjt.v10.i2.29.
Transplant recipients are vulnerable to a higher risk of malignancy after solid organ transplantation and allogeneic hematopoietic stem-cell transplant. Post-transplant lymphoproliferative disorders (PTLD) include a wide spectrum of diseases ranging from benign proliferation of lymphoid tissues to frank malignancy with aggressive behavior. Two main risk factors of PTLD are: Firstly, the cumulative immunosuppressive burden, and secondly, the oncogenic impact of the Epstein-Barr virus. The latter is a key pathognomonic driver of PTLD evolution. Over the last two decades, a considerable progress has been made in diagnosis and therapy of PTLD. The treatment of PTLD includes reduction of immunosuppression, rituximab therapy, either isolated or in combination with other chemotherapeutic agents, adoptive therapy, surgical intervention, antiviral therapy and radiotherapy. In this review we shall discuss the prevalence, clinical clues, prophylactic measures as well as the current and future therapeutic strategies of this devastating disorder.
实体器官移植和异基因造血干细胞移植后,移植受者患恶性肿瘤的风险更高。移植后淋巴细胞增殖性疾病(PTLD)包括一系列疾病,从淋巴组织的良性增殖到具有侵袭性的明显恶性肿瘤。PTLD的两个主要危险因素是:第一,累积的免疫抑制负担;第二,爱泼斯坦-巴尔病毒的致癌作用。后者是PTLD演变的关键病理学驱动因素。在过去二十年中,PTLD的诊断和治疗取得了相当大的进展。PTLD的治疗包括减少免疫抑制、利妥昔单抗治疗(单独或与其他化疗药物联合使用)、过继性治疗、手术干预、抗病毒治疗和放疗。在本综述中,我们将讨论这种毁灭性疾病的患病率、临床线索、预防措施以及当前和未来的治疗策略。