Progressive Multifocal Leukoencephalopathy After Therapy for Chronic Lymphocytic Leukemia

Jacob Laubach
{"title":"Progressive Multifocal Leukoencephalopathy After Therapy for Chronic Lymphocytic Leukemia","authors":"Jacob Laubach","doi":"10.3816/CLK.2009.n.011","DOIUrl":null,"url":null,"abstract":"<div><p>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.</p></div>","PeriodicalId":100271,"journal":{"name":"Clinical Leukemia","volume":"3 2","pages":"Pages E24-E26"},"PeriodicalIF":0.0000,"publicationDate":"2009-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3816/CLK.2009.n.011","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Leukemia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S193169251360011X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Editorial Board Blood and Bone Marrow Transplantation for Acute Myeloid Leukemia Genomic Lesions Involved in Chronic Myeloid Leukemia Progression Acute Leukemia with M3 Morphology Without Cytogenetic Abnormalities Related to Acute Promyelocytic Leukemia: Description of a Refractory Pediatric Case Salvage of Donor Graft with Decitabine and Maintenance Post Allogeneic Stem Cell Transplantation in Myelodysplastic/Myeloproliferative Disease: A Case Report
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1