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CD56-Negative Aggressive NK Cell Leukemia Relapsing as Multiple Cranial Nerve Palsies: Case Report and Literature Review

机译:CD56阴性侵袭性NK细胞白血病复发为多发性颅神经麻痹:病例报告和文献综述

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摘要

Background Aggressive natural killer cell leukemia (ANKL) is extremely rare and habitually manifests as a systemic disease with multiorgan failure that rapidly evolves to death. The neoplastic natural killer (NK) cells usually harbor the Epstein-Barr virus (EBV) with a latent viral infection pattern type II; they often have a cytoplasmic CD3ε+ and surface CD3, CD2+, and CD56+ immunophenotype, and they show complex genetic abnormalities affecting multiple tumor suppressor genes and oncogenes. We present a rare case of CD56-negative ANKL and review the clinical and laboratorial criteria for the diagnosis, as well as the available therapies.
机译:背景攻击性自然杀伤细胞白血病(ANKL)非常罕见,习惯上表现为全身性疾病,多器官功能衰竭迅速发展为死亡。肿瘤自然杀伤(NK)细胞通常带有带有潜在II型病毒感染模式的爱泼斯坦-巴尔病毒(EBV)。它们通常具有胞质CD3ε + 和表面CD3 -,CD2 + 和CD56 + 免疫表型,显示复杂的遗传异常会影响多个抑癌基因和癌基因。我们介绍了CD56阴性的ANKL的罕见病例,并回顾了诊断的临床和实验室标准以及可用的治疗方法。

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