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首页> 外文期刊>Leukemia and lymphoma >Successful treatment of posttransplant lymphoproliferative disorder in a renal transplant patient by autologous peripheral blood stem cell transplantation.
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Successful treatment of posttransplant lymphoproliferative disorder in a renal transplant patient by autologous peripheral blood stem cell transplantation.

机译:通过自体外周血干细胞移植成功治疗肾移植患者的移植后淋巴增生性疾病。

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摘要

Posttransplant lymphoproliferative disorder (PTLD), a well recognized complication of organ transplantation, comprises a wide spectrum of heterogeneous lymphoid proliferations ranging from self-limiting mononucleosis through aggressive monoclonal non-Hodgkin's lymphoma (NHL). There has been marginal success in treating PTLD using a number of treatment modalities, including combination chemotherapy. There have been few reports of the use of high dose chemotherapy with stem cell rescue as a treatment for PTLD. We report a renal allograft recipient who developed PTLD of the diffuse large cleaved B cell, NHL type. Reduction of immunosuppression was initially effective, however the patient relapsed, and was treated successfully with CHOP chemotherapy. Two years later he again relapsed and was treated with high dose melphalan followed by autologous peripheral blood stem cell transplantation (PSCT). The patient has remained in complete remission for 4 years with no major organ toxicities and a functioning renal allograft on minimal immunosuppression. This case illustrates a potential role for high dose chemotherapy with stem cell transplantation for the treatment of PTLD.
机译:移植后淋巴组织增生性疾病(PTLD)是公认的器官移植并发症,包括广泛的异类淋巴样增生,范围从自限性单核细胞增多症到侵袭性单克隆非霍奇金淋巴瘤(NHL)。使用多种治疗方式(包括联合化疗)治疗PTLD取得了一定的成功。很少有报道将高剂量化疗与干细胞抢救一起用作PTLD的治疗方法。我们报告了肾同种异体移植受者谁发展了弥漫性大分裂的B细胞,NHL型的PTLD。减少免疫抑制起初是有效的,但是患者复发了,并已通过CHOP化疗成功治疗。两年后,他再次复发,接受高剂量马法兰治疗,然后进行自体外周血干细胞移植(PSCT)。该患者已完全缓解4年,无主要器官毒性,并且仅在最低免疫抑制下即可正常移植肾。该病例说明了高剂量化学疗法与干细胞移植治疗PTLD的潜在作用。

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