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Published on: January 19, 2019
Transiently reduced water diffusion in the corpus callosum in infants with benign partial epilepsy in infancy
Akihisa Okumura1, Shinpei Abe, Satoshi Hara
1Department of Pediatrics, Juntendo University, School of Medicine, Bunkyo-ku, Tokyo, 113-8421, Japan. okumura@juntendo.ac.jp
Insights
Transient diffusion reduction in the corpus callosum was observed in infants with benign partial epilepsy. These findings in neuroimaging were temporary and linked to seizure clusters in children.
Area of Science:
- Pediatric Neurology
- Neuroimaging
- Epilepsy
Background:
- Benign partial epilepsy in infancy typically presents with normal neuroimaging findings.
- This study investigates atypical neuroimaging observations in this condition.
Observation:
- Two infants with probable benign partial epilepsy presented with seizure clusters.
- Standard neurological examinations and interictal electroencephalography were normal.
- Diffusion-weighted MRI revealed transient abnormalities in the corpus callosum.
Findings:
- A temporary reduction in water diffusion was noted in the genu and splenium of the corpus callosum in one patient, and in the splenium only in the second patient.
- These diffusion abnormalities resolved on follow-up MRI.
- The observed callosal lesions were transient and not associated with developmental delays or interictal neurological deficits.
Implications:
- Transient callosal lesions on diffusion-weighted MRI may be associated with seizure clusters in benign partial epilepsy of infancy.
- This finding could refine diagnostic approaches and understanding of epilepsy pathophysiology in infants.
- Further research is warranted to explore the relationship between transient white matter changes and epileptic activity.
Abstract:
Neuroimaging findings are usually normal in children with benign partial epilepsy in infancy. However, we found a transient reduction of water diffusion in the corpus callosum in two patients with probable benign partial epilepsy in infancy. The patients were admitted to our hospital because of seizure clusters. No delay in the developmental milestones was seen, and no neurological abnormalities were observed during the interictal period. Interictal electroencephalography was normal in both infants. However, the diffusion-weighted images showed abnormal high intensities in both the genu and splenium in one patient and in the splenium only in the other. No diffusion abnormalities were observed in follow-up magnetic resonance imaging. The clustered seizures may be related to the transient callosal lesions seen in our patients.
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