Key result
Brain MR imaging in 6 infants with human parechovirus meningoencephalitis consistently demonstrated low diffusivity within the thalami, corpus callosum, and subcortical white matter.
Why the study?
Human parechovirus is an increasingly recognized cause of neonatal meningoencephalitis, and identifying characteristic brain MR imaging abnormalities alongside PCR testing could allow specific diagnosis and avoid costly further evaluation.
What are the characteristic brain MR imaging abnormalities in infants with human parechovirus meningoencephalitis?
Case Report (n=6)
What are the characteristic brain MR imaging abnormalities in infants with human parechovirus meningoencephalitis?
Distinctive MR imaging patterns in infants with human parechovirus meningoencephalitis can aid in specific diagnosis when combined with PCR testing.
Human parechovirus infection is an increasingly recognized cause of neonatal meningoencephalitis. We describe characteristic clinical features and brain MR imaging abnormalities of human parechovirus meningoencephalitis in 6 infants. When corroborated by increasingly available polymerase chain reaction-based testing of the CSF, the distinctive MR imaging appearance may yield a specific diagnosis that obviates costly and time-consuming further clinical evaluation. In our study, infants with human parechovirus presented in the first 35 days of life with seizures, irritability, and sepsis. MR imaging consistently demonstrated low diffusivity within the thalami, corpus callosum, and subcortical white matter with a frontoparietal predominance. T1 and T2 shortening connoting white matter injury along the deep medullary veins suggests venous ischemia as an alternative potential pathogenetic mechanism to direct neuroaxonal injury.
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Sarma et al. (2019) conducted a case report in Human parechovirus meningoencephalitis (n=6). Brain MR imaging was evaluated on Brain MR imaging abnormalities. Brain MR imaging in 6 infants with human parechovirus meningoencephalitis consistently demonstrated low diffusivity within the thalami, corpus callosum, and subcortical white matter.
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