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Published on: July 19, 2019
Cerebellar progressive multifocal leucoencephalopathy identified by the shrimp sign
Vinit Suri1, Ajay Kumar Sinha2, Mayank Priyaranjan2
1Neurology, Indraprastha Apollo Hospitals New Delhi, New Delhi, New Delhi, India vinitsuri@hotmail.com.
Abstract:
Progressive multifocal leucoencephalopathy (PML) is a demyelinating disease caused by the John Cunningham (JC) virus, which may get reactivated under certain immunosuppressive states such as AIDS, immunomodulatory therapy and haematological malignancies. PML has been reported rarely even in immunocompetent individuals where no immunodeficiency was present. PML characteristically involves periventricular and juxtacortical white matter. Isolated cerebellar or brainstem PML may be seen rarely. We present a case of a man in his 70s who presented with rapidly progressive cerebellar ataxia, ptosis and bipyramidal signs. Investigations excluded a direct viral cerebellar infection, acute disseminated encephalomyelitis, paraneoplastic cerebellar degeneration or any structural cerebellar lesion. MRI PET study revealed the classical shrimp sign which raised the possibility of cerebellar PML, and the same was confirmed by a positive JC virus PCR in the cerebrospinal fluid. Our patient had no known immune-compromising state, but further workup revealed a low CD4 count suggestive of idiopathic CD4 lymphopenia. The case illustrates the importance of the shrimp sign on MRI, the possibility of cerebellar involvement of PML as well as the need to consider a differential diagnosis of PML even in individuals with no obvious immunocompromised state.
Insights
Progressive multifocal leucoencephalopathy (PML) can occur in individuals without apparent immune compromise. This case highlights cerebellar PML and the diagnostic significance of the "shrimp sign" in MRI scans.
Area of Science:
- Neurology
- Virology
- Immunology
Background:
- Progressive multifocal leucoencephalopathy (PML) is a rare demyelinating disease caused by the John Cunningham (JC) virus.
- JC virus reactivation is typically associated with immunosuppressive states like AIDS, immunomodulatory therapy, or hematological malignancies.
- PML commonly affects periventricular and juxtacortical white matter, with isolated cerebellar or brainstem involvement being rare.
Observation:
- A case study of a man in his 70s presenting with rapidly progressive cerebellar ataxia, ptosis, and bipyramidal signs.
- Initial investigations ruled out other causes such as viral cerebellar infections, ADEM, paraneoplastic cerebellar degeneration, or structural lesions.
- MRI PET revealed a characteristic "shrimp sign," suggesting cerebellar PML.
Findings:
- Cerebrospinal fluid (CSF) analysis confirmed PML through positive JC virus PCR.
- The patient had no known immunocompromised state, but was found to have idiopathic CD4 lymphopenia.
- This case demonstrates cerebellar PML in an individual without overt immunosuppression.
Implications:
- The "shrimp sign" on MRI is a crucial diagnostic indicator for cerebellar PML.
- PML should be considered in the differential diagnosis even in immunocompetent individuals presenting with relevant neurological symptoms.
- Idiopathic CD4 lymphopenia can be an underlying factor in PML development, emphasizing the need for thorough immune workup.
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