进行性多灶性白质脑病
医学
血液学
美罗华
背景(考古学)
JC病毒
脱髓鞘病
疾病
内科学
白质脑病
苯达莫司汀
肿瘤科
重症监护医学
神经学
淋巴瘤
免疫学
病毒
古生物学
精神科
生物
作者
Panagiotis Diamantopoulos,Konstantinos Kalopisis,Aikaterini Tsatsou,Athina Efthymiou,Nefeli Giannakopoulou,Sevastianos Hatzidavid,Nora‐Athina Viniou
摘要
Progressive multifocal leukoencephalopathy (PML) is a rare, often fatal demyelinating disease of the central nervous system (CNS) caused by the reactivation of JC polyomavirus in the CNS. We present a case of a 54-year-old man with follicular lymphoma diagnosed with PML after being treated with anti-CD20 monoclonal antibody-based regimens for several years. Due to the lack of effective treatment choices for PML, the patient was treated with nivolumab, based on recent reports, but succumbed to his disease a few months after diagnosis. In this paper, we focus on reviewing the literature of PML cases correlated with newer agents used in hematology, possible factors affecting disease prognosis, as well as the available data on upcoming therapeutic options for patients with PML. Though newer promising treatments such as anti-PD1 monoclonal antibodies arise, a definitive treatment option is yet to be found. Vigilance, early detection, and prompt intervention play a crucial role in the prognosis of PML in patients with hematological malignancies.
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