A Case Report of Progressive Multifocal Leukoencephalopathy (PML) in an Immunocompetent Patient

Progressive multifocal leukoencephalopathy (PML) is a rare but fatal demyelinating disorder resulting from reactivation of latent John Cunningham virus (JCV), which induces demyelinating lytic infection of oligodendrocytes. We report a case of PML in an individual without identifiable immunodeficiency who presented with insidious and progressive deficits in speech and motor function. Diagnostic workup revealed JC viral DNA in cerebrospinal fluid, and magnetic resonance imaging (MRI) demonstrated multiple asymmetric lesions within the subcortical and deep white matter. Despite administration of the immune checkpoint inhibitor pembrolizumab, the patient's neurological status continued to decline, culminating in death. This case underscores the necessity of considering PML in the differential diagnosis of patients lacking classic risk factors when clinical presentation and neuroimaging findings are indicative of demyelinating pathology.

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Publication Details

Journal
Cureus
Published
2025-09-02
DOI
https://doi.org/10.7759/cureus.91491
Citations
1
Primary Topic
Polyomavirus and related diseases
Type
article
Field-Weighted Citation Impact
1.05
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article

A Case Report of Progressive Multifocal Leukoencephalopathy (PML) in an Immunocompetent Patient

El-Sayed A. El-Sheikh, Nágela Maria Henrique Mascarenhas, S. M. S. M. Rezwanuzzaman, Sunil Kumar et al.
1 citations
Cureus
Polyomavirus and related diseases
1.05
article

A Case Report of Progressive Multifocal Leukoencephalopathy (PML) in an Immunocompetent Patient

El-Sayed A. El-Sheikh, Nágela Maria Henrique Mascarenhas, S. M. S. M. Rezwanuzzaman, Sunil Kumar, Kazi Subrina Nazneen
article en
1 citations

Abstract

Progressive multifocal leukoencephalopathy (PML) is a rare but fatal demyelinating disorder resulting from reactivation of latent John Cunningham virus (JCV), which induces demyelinating lytic infection of oligodendrocytes. We report a case of PML in an individual without identifiable immunodeficiency who presented with insidious and progressive deficits in speech and motor function. Diagnostic workup revealed JC viral DNA in cerebrospinal fluid, and magnetic resonance imaging (MRI) demonstrated multiple asymmetric lesions within the subcortical and deep white matter. Despite administration of the immune checkpoint inhibitor pembrolizumab, the patient's neurological status continued to decline, culminating in death. This case underscores the necessity of considering PML in the differential diagnosis of patients lacking classic risk factors when clinical presentation and neuroimaging findings are indicative of demyelinating pathology.

CureusVol. 17(9)
Medway NHS Foundation Trust (GB)
Openalex Percentile: Top 18%
Polyomavirus and related diseases
1.05
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