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Transient encephalopathy with reversible white matter lesions: a case report
Atsushi Yokoyama1, Yoshiaki Saito, Fumihide Kato
1Department of Pediatrics, Shimane Prefectural Central Hospital, Himehara 4-1-1, Izumo, Shimane 693-8555, Japan. atsushiy@grape.med.tottori-u.ac.jp
Insights
A child with optic nerve hypoplasia experienced febrile seizures and temporary white matter changes on MRI. Despite recovery, developmental delays persisted, highlighting the need for careful diagnosis.
Area of Science:
- Neurology
- Pediatrics
- Neuroimaging
Background:
- Bilateral optic nerve hypoplasia (ONH) is a congenital condition affecting vision.
- Mild psychomotor retardation can be associated with ONH.
- Febrile convulsions are common in young children.
Observation:
- A 1-year-9-month-old boy with ONH and psychomotor delays presented with seizures and unconsciousness.
- Diffusion-weighted MRI showed transient high signal intensity in deep cerebral white matter and corpus callosum.
- These MRI abnormalities resolved within five days.
Findings:
- The patient experienced a complete recovery from the acute episode.
- Follow-up MRI at six months showed no residual atrophy or abnormalities.
- Despite clinical recovery, the child exhibited persistent developmental delays.
Implications:
- This case highlights the importance of considering transient white matter changes in the differential diagnosis of pediatric neurological events.
- The findings underscore the potential for long-term developmental consequences even after acute symptom resolution in children with underlying conditions like ONH.
- Further research into the neurobiological mechanisms linking transient white matter changes to developmental outcomes is warranted.
Abstract:
We report on a boy with bilateral optic nerve hypoplasia and mild psychomotor retardation. At 1 year and 9 months of age, he was admitted to hospital with a cluster of febrile convulsions and unconsciousness. Magnetic resonance imaging (MRI) revealed widespread areas of high signal intensity on diffusion-weighted imaging of the deep cerebral white matter and corpus callosum. This imaging disappeared at five days of illness. No atrophy or abnormalities were noted on the 6-month follow-up MRI. Despite full recovery after the acute episode, the patient showed retarded developmental progress. We discuss the differential diagnosis for this case.
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