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Autoimmune Lymphoproliferative Syndrome and Epstein-Barr Virus-Associated Lymphoma: An Adjunctive Diagnostic Role for Monitoring EBV Viremia?

机译:自身免疫性淋巴增生综合征和爱泼斯坦-巴尔病毒相关淋巴瘤:监测EBV病毒血症的辅助诊断作用?

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Background. Autoimmune lymphoproliferative syndrome (ALPS) is a genetic disorder of lymphocyte homeostasis due to defects in FAS-mediated apoptosis. ALPS is characterized by childhood onset of chronic lymphadenopathy and splenomegaly, autoimmunity, an expanded population of double-negative T cells (DNTCs), and an increased risk of lymphoma. This propensity for lymphoma in ALPS is not well understood. It is possible that lymphomagenesis in some of these patients may result from Epstein-Barr virus (EBV) infection exploiting the defective T-cell surveillance resulting from impaired FAS-mediated apoptosis.Case Presentation. We report the first case, to our knowledge, of lymphoma in a patient with ALPS that was clinically heralded by progressively increasing EBV viremia. We discuss its practical implications and the possible immune pathways involved in the increased risk for EBV-associated lymphoproliferative disorders in ALPS patients.Conclusion. In patients with ALPS, distinguishing chronic lymphadenopathy from emerging lymphoma is difficult, with few practical recommendations available. This case illustrates that, at least for some patients, monitoring for progressively increasing EBV viremia may be useful.
机译:背景。自身免疫性淋巴组织增生综合症(ALPS)是由于FAS介导的细胞凋亡缺陷而引起的淋巴细胞稳态的遗传性疾病。 ALPS的特征是儿童时期开始出现慢性淋巴结肿大和脾肿大,自身免疫,双阴性T细胞(DNTC)人口增加以及淋巴瘤的风险增加。人们对ALPS中淋巴瘤的这种倾向还不甚了解。这些患者中的一些淋巴瘤的发生可能是由爱泼斯坦巴尔病毒(EBV)感染导致的,该感染利用了FAS介导的细胞凋亡受损导致的T细胞监视缺陷。据我们所知,我们报道的第一例淋巴瘤是ALPS患者,该患者在临床上通过逐渐增加的EBV病毒血症而得到预示。我们讨论了其实际意义以及与ALPS患者发生EBV相关的淋巴增生性疾病风险增加有关的可能的免疫途径。在ALPS患者中,很难将慢性淋巴结病与新发淋巴瘤区分开,几乎没有实用的建议。这种情况说明,至少对于某些患者,监测逐渐增加的EBV病毒血症可能是有用的。

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