JC virus granule cell neuronopathy

Case contributed by Damien Charles
Diagnosis almost certain

Presentation

The patient has been experiencing ataxia for a few weeks and is being monitored due to HIV infection.

Patient Data

Age: 40 years
Gender: Female

Initial MRI

mri

Coronal T2 MRI scan shows subtle atrophy of the right cerebellum without signal intensity abnormality.

A few months later

mri

There is worsening of right cerebellar volume loss and subtle areas of high signal in right MCP on axial FLAIR.

1 year later

mri

18 months later

mri

Despite undetectable viral load, radiologic findings have worsened:

Case Discussion

Clinical presentation, history of HIV infection, cerebellar symptoms, laboratory tests (PCR JC Virus), and radiological findings are nearly pathognomonic of JC virus granule cell neuronopathy.

Granule cell neuronopathy (GCN) is a rare form of CNS JC virus disease first described by Du Pasquier et al. in 2003 and later by Koralnik et al. in 2005. It mainly occurs in immunocompromised patients and is characterized by selective infection of the cerebellar granule cell layer. Patients with GCN typically present with cerebellar symptoms, while imaging studies show cerebellar atrophy and/or signal changes.

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