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首页> 外文期刊>Diagnostic pathology >EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report
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EBV-associated post-transplantation B-cell lymphoproliferative disorder following allogenic stem cell transplantation for acute lymphoblastic leukaemia: tumor regression after reduction of immunosuppression - a case report

机译:同种异体干细胞移植后与EBV相关的B细胞淋巴细胞增生性疾病治疗急性淋巴细胞白血病:免疫抑制降低后肿瘤消退-病例报告

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摘要

Epstein-Barr virus (EBV)-associated B-cell post-transplantation lymphoproliferative disorder (PTLD) is a severe complication following stem cell transplantation. This is believed to occur as a result of iatrogenic immunosuppression leading to a relaxation of T-cell control of EBV infection and thus allowing viral reactivation and proliferation of EBV-infected B-lymphocytes. In support of this notion, reduction of immunosuppressive therapy may lead to regression of PTLD. We present a case of an 18-year-old male developing a monomorphic B-cell PTLD 2 months after receiving an allogenic stem cell transplant for acute lymphoblastic leukemia. Reduction of immunosuppressive therapy led to regression of lymphadenopathy. Nevertheless, the patient died 3 months afterwards due to extensive graft-vs.-host-disease and sepsis. As a diagnostic lymph node biopsy was performed only after reduction of immunosuppressive therapy, we are able to study the histopathological changes characterizing PTLD regression. We observed extensive apoptosis of blast cells, accompanied by an abundant infiltrate comprising predominantly CD8-positive, Granzyme B-positive T-cells. This observation supports the idea that regression of PTLD is mediated by cytotoxic T-cells and is in keeping with the observation that T-cell depletion, represents a major risk factor for the development of PTLD.
机译:与爱泼斯坦巴尔病毒(EBV)相关的B细胞移植后淋巴细胞增生性疾病(PTLD)是干细胞移植后的严重并发症。据认为,这是由于医源性免疫抑制导致放松对EBV感染的T细胞控制而导致的,从而允许病毒重新激活和感染EBV的B淋巴细胞增殖。为了支持这一观点,减少免疫抑制疗法可能导致PTLD退步。我们介绍了一个18岁男性在接受异体干细胞移植治疗急性淋巴细胞性白血病2个月后发展为单形B细胞PTLD的情况。免疫抑制疗法的减少导致淋巴结病的消退。然而,由于广泛的移植物抗宿主疾病和败血症,患者在3个月后死亡。由于仅在减少免疫抑制疗法后才进行诊断性淋巴结活检,因此我们能够研究表征PTLD退化的组织病理学变化。我们观察到胚细胞的广泛凋亡,并伴随着大量的浸润,包括主要是CD8阳性,粒酶B阳性T细胞。该观察结果支持以下观点:PTLD的退化是由细胞毒性T细胞介导的,并且与T细胞耗竭是PTLD发展的主要危险因素的观察结果相吻合。

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