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. 2020 Nov 20;17(1):37–51. doi: 10.1038/s41582-020-00427-y

Table 1.

Summary of diagnostic criteria for PML

Path to diagnosis Diagnostic features Diagnosisa
Definite PML Probable PML Possible PML Not PML
Neuropathological Histopathological triad of demyelination, bizarre astrocytes, and enlarged oligodendroglial nuclei Histopathological triad with detection of JCV protein and/or JCV DNA Histopathological triad only Detection of JCV protein only No histopathological evidence of JCV infection
JCV protein detected in focal brain lesions by immunohistochemistry or electron microscopy
JCV DNA detected in focal brain lesions by in situ hybridization or PCR
Combined clinical, radiological and laboratory Clinical: progressive neurological symptoms JCV DNA detected in the CSF, and both imaging features and clinical features present JCV DNA detected in the CSF and either imaging or clinical features present Imaging and clinical features only, or only detection of JCV DNA in the CSF Isolated clinical or imaging features
Imaging: MRI features
Laboratory: JCV DNA detected in the CSF by PCR

CSF, cerebrospinal fluid; JCV, JC virus; PCR, polymerase chain reaction; PML, progressive multifocal leukoencephalopathy. aCriteria are compiled from ref.64.