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Concurrent Epstein-Barr virus associated NK/T cell lymphoma after immunosuppressive therapy for aplastic anemia: report of a case and review of literature

机译:免疫抑制治疗再生障碍性贫血后并发爱泼斯坦-巴尔病毒相关的NK / T细胞淋巴瘤:病例报告和文献复习

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摘要

Aplastic anemia (AA) patients with prolonged immunosuppression have a risk of development of lymphoproliferative disorders (LPDs), especially combined with Epstein-Barr virus (EBV) infection. However, development of nature killer/T (NK/T) cell lymphoma, in a nontransplantation setting, has not been documented for AA patients with immunosuppressive therapy (IST). Herein, we described a middle-aged man, Han ethnic, who presented with swelled parotid gland after a long history of IST for AA. Fever, night sweating, weight loss had not been found. Increased heterotypic lymphocytes had been detected in the left side of parotid gland demonstrated as cCD3+, CD56+, GranB+, TIA-1+, MUM-1+, KI-67 (50%-75%)++, Bcl-6-, MPO- by immunohistochemistry, and in-situ hybridization (ISH) indicated EBER positive. Chromosome analysis by R banding method revealed 46, XY [20]. NK/T cell lymphoma concurrent with aplastic anemia was diagnosed and a mild chemotherapy regimen including vincristine, prednisone, L-asparaginase was administered. The parotid mass was gradually regressed after the first cycle of chemotherapy. The patient discharged from the hospital voluntarily and lost the follow-up.
机译:免疫抑制时间延长的再生障碍性贫血(AA)患者有发生淋巴增生性疾病(LPD)的风险,特别是与爱泼斯坦-巴尔病毒(EBV)感染并存。然而,对于非免疫治疗的机管局(AA)患者,非移植性自然杀伤/ T(NK / T)细胞淋巴瘤的发展尚未见报道。在这里,我们描述了一个中年男子汉族,他在接受IST的IST悠久历史后出现了腮腺肿胀。尚未发现发烧,盗汗,体重减轻。在腮腺左侧检测到异型淋巴细胞增多,表现为cCD3 + ,CD56 + ,GranB + ,TIA-1 + ,MUM-1 + ,KI-67(50%-75%) ++ ,Bcl-6 - ,MPO -(通过免疫组织化学)和原位杂交(ISH)表明EBER阳性。通过R谱带法进行的染色体分析显示46,XY [20]。诊断为NK / T细胞淋巴瘤并发再生障碍性贫血,并给予温和的化疗方案,包括长春新碱,泼尼松,L-天冬酰胺酶。在第一轮化疗后,腮腺肿块逐渐消退。该患者自愿出院并失去随访。

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