Progressive multifocal leucoencephalopathy as a rare complication of anti-synthetase syndrome associated with immunosuppressive therapy
Related Experiment Video
Updated: Mar 21, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Shakila Fatehpoor1, James Milton2
1Stroke, Maidstone and Tunbridge Wells NHS Trust, Maidstone, UK shakila.fatehpoor@nhs.net.
Abstract:
We present the case of a woman in her late 50s with anti-synthetase syndrome who developed progressive multifocal leucoencephalopathy (PML), a rare and potentially fatal complication of immunosuppressive therapy. She was admitted with transient left-sided paraesthesia, left hand weakness and incoordination, and intermittent blurry vision, initially suspected to be a cerebrovascular event. Imaging revealed multifocal subcortical white matter lesions, and brain biopsy confirmed PML. Notably, she had been treated with mycophenolate mofetil and low-dose prednisolone, without rituximab. Her symptoms improved following the cessation of immunosuppressive therapy. This case highlights the importance of considering PML in immunosuppressed patients presenting with neurological symptoms, even in the absence of monoclonal antibody exposure, and suggests a possible association with conventional immunosuppressive therapy, although causality cannot be established from a single observation.
More Related Videos
06:19Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
Published on: September 9, 2022
10:50Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo
Published on: March 26, 2019
Related Concept Videos
Nephrotic Syndrome I : Introduction
Nephrotic Syndrome II : Assessment and Medical Management
Nephrotic Syndrome III : Nursing Management