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Subacute sclerosing panencephalitis with bilateral inferior collicular hyperintensity on magnetic resonance imaging
Maya Thomas1, Ajith Sivadasan, Mathew Alexander
1Department of Neurological Sciences, Section of Neurology, Christian Medical College, Vellore, Tamil Nadu, India.
Abstract:
Subacute sclerosing panencephalitis (SSPE) is chronic encephalitis occurring after infection with measles virus. An 8-year-old boy presented with progressive behavioral changes, cognitive decline and myoclonic jerks, progressing to a bed bound state over 2 months. Magnetic resonance imaging (MRI) brain showed T2-weighted hyperintensities in the subcortical areas of the left occipital lobe and brachium of the inferior colliculus on both sides. EEG showed bilateral, synchronous periodic discharges. Serum/cerebrospinal fluid measles IgG titer was significantly positive. The overall features were suggestive of SSPE. MRI finding of bilateral inferior colliculus changes on MRI without significant involvement of other commonly involved areas suggests an uncommon/rare imaging pattern of SSPE.
Insights
Subacute sclerosing panencephalitis (SSPE), a rare complication of measles virus infection, presents with rapid neurological decline. This case highlights an uncommon MRI pattern in the inferior colliculi, crucial for diagnosing this severe encephalitis.
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Subacute sclerosing panencephalitis (SSPE) is a rare, progressive, and fatal neurological complication following measles virus infection.
- It typically affects children and young adults, leading to severe cognitive and motor deficits.
Observation:
- An 8-year-old boy exhibited rapid onset of behavioral changes, cognitive decline, and myoclonic jerks over two months.
- Brain MRI revealed T2-weighted hyperintensities in subcortical occipital lobes and bilateral inferior colliculi.
- Electroencephalogram (EEG) demonstrated bilateral, synchronous periodic discharges.
Findings:
- Serum and cerebrospinal fluid measles IgG titers were significantly elevated, confirming measles virus infection.
- The clinical and EEG findings were highly suggestive of SSPE.
- The MRI pattern, particularly bilateral inferior colliculus involvement without typical white matter lesions, represents an uncommon imaging presentation of SSPE.
Implications:
- This case underscores the importance of considering SSPE in pediatric patients with rapid neurological deterioration, even with atypical imaging findings.
- Recognizing rare MRI patterns of SSPE is critical for timely diagnosis and management.
- Further research into the varied neuroimaging manifestations of SSPE could improve diagnostic accuracy.
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