Progressive Multifocal Leukoencephalopathy: Literature Review and Clinical Case Study
https://doi.org/10.37174/2587-7593-2024-7-4-54-61
Abstract
Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system, primarily affecting individuals with severe immunosuppression. Its subacute onset, nonspecific clinical manifestations, and MRI findings complicate accurate and timely diagnosis. This review provides a brief overview of the etiology and fundamental pathogenesis of the disease, demonstrating through a clinical case the importance of a multimodal approach and the potential challenges in the differential diagnosis of PML.
About the Authors
K. V. GolanovaRussian Federation
Kristina V. Golanova
24, bld. 1, Petrovka str., Moscow, Russia 127051
Competing Interests:
Conflict of interests. Not declared
D. V. Sashin
Russian Federation
24 Kashirskoe Shosse, Moscow, Russia 115478
Competing Interests:
Conflict of interests. Not declared
E. A. Nechipay
Russian Federation
24 Kashirskoe Shosse, Moscow, Russia 115478
Competing Interests:
Conflict of interests. Not declared
N. V. Garanina
Russian Federation
24 Kashirskoe Shosse, Moscow, Russia 115478
Competing Interests:
Conflict of interests. Not declared
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Review
For citations:
Golanova K.V., Sashin D.V., Nechipay E.A., Garanina N.V. Progressive Multifocal Leukoencephalopathy: Literature Review and Clinical Case Study. Journal of oncology: diagnostic radiology and radiotherapy. 2024;7(4):54-61. (In Russ.) https://doi.org/10.37174/2587-7593-2024-7-4-54-61