Progressive Multifocal Leukoencephalopathy After Therapy for Chronic Lymphocytic Leukemia

Jacob Laubach
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引用次数: 1

Abstract

Progressive multifocal leukoencephalopathy (PML) is a lethal degenerative disorder of the central nervous system caused by reactivation of latent polyomavirus JC in the immunosuppressed host. Although the condition is most prevalent among individuals with HIV, it also occurs in association with other diseases and therapies that compromise immune function, including lymphoproliferative disorders (LPDs) treated with chemotherapy. Herein, the clinical course of an individual with chronic lymphocytic leukemia who developed PML after treatment with fludarabine, cyclophosphamide, and rituximab is described. The report highlights diagnostic challenges posed by nonspecific neurologic symptoms and radiographic findings that can be associated with PML. The ensuing discussion describes important discoveries that have contributed to the understanding of PML, clinical and diagnostic characteristics of the disease, specific features of LPD-associated PML, and treatment strategies for this condition.

慢性淋巴细胞白血病治疗后进行性多灶性白质脑病
进行性多灶性白质脑病(PML)是一种致命的中枢神经系统退行性疾病,由免疫抑制宿主体内潜伏多瘤病毒JC的再激活引起。尽管这种情况在艾滋病毒感染者中最为普遍,但它也与其他损害免疫功能的疾病和疗法有关,包括用化疗治疗的淋巴细胞增生性疾病(lpd)。本文描述了一位慢性淋巴细胞白血病患者在接受氟达拉滨、环磷酰胺和利妥昔单抗治疗后发生PML的临床过程。该报告强调了与PML相关的非特异性神经系统症状和影像学表现所带来的诊断挑战。随后的讨论描述了有助于理解PML的重要发现,疾病的临床和诊断特征,lpd相关PML的具体特征,以及这种疾病的治疗策略。
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