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Narrative review outlines diagnostic framework for PML in immunocompromised patients.

Narrative review outlines diagnostic framework for PML in immunocompromised patients.
Photo by Cht Gsml / Unsplash
Key Takeaway
Consider this framework to aid timely PML diagnosis in immunocompromised patients, noting its limitations.

This is a narrative review that proposes a diagnostic framework for progressive multifocal leukoencephalopathy (PML) in immunocompromised individuals, aiming to differentiate it from common mimics in clinical practice. The authors synthesize key arguments for timely recognition and expedited diagnosis, emphasizing clinical and radiographic patterns. The review does not report pooled effect sizes or trial-level data, as it is a qualitative synthesis.

The authors note significant limitations, including the low incidence of PML, which leads to a lack of clinical familiarity, diverse clinical manifestations, and radiographic overlap with other disorders. These factors complicate diagnosis and are central to the review's discussion.

The practice relevance is to aid neurologists in timely recognition and expedited diagnosis. The review explicitly states that novel and experimental therapies are beyond its scope. No specific study populations, interventions, comparators, or adverse events are described, as these details are not reported in the source.

Overall, the framework is presented as a clinical aid, but its application is constrained by the inherent challenges of PML diagnosis. The authors' arguments are qualitative and based on clinical experience and existing literature, not new empirical data.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMar 2026
View Original Abstract ↓
Progressive multifocal leukoencephalopathy (PML) is a rare, often fatal demyelinating disease of the central nervous system caused by reactivation of latent JC virus in immunocompromised individuals. Despite advances in understanding its pathogenesis, PML remains a diagnostic challenge due to its diverse clinical manifestations, radiographic overlap with other disorders, low incidence and subsequent lack of clinical familiarity. Diagnostic delays, often extending months after symptom onset, are common and contribute to poor outcomes. This review outlines the key clinical features, risk factors, diagnostic and neuroradiographic findings of PML to aid practicing neurologists in timely recognition and expedited diagnosis. We review emerging biomarkers and advanced diagnostic tools to identify PML. We also compare PML with its common mimics to underscore diagnostic pitfalls and how to overcome them. Novel and experimental therapies are beyond the scope of this article; instead, we focus on equipping neurologists with a framework grounded in patient data and clinical experience to establish timely diagnoses of PML.
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