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Published on: July 24, 2016
A severe neurological complication of influenza in a previously well child
Philippa McSwiney1, Jessica Purnama2, Andrew Kornberg3
1Department of General Medicine, The Royal Children's Hospital, Melbourne, Victoria, Australia.
Insights
A rare case of acute necrotising encephalopathy (ANE) in a child caused by influenza A highlights the severe risks of this infection. Genetic factors, like the RANBP2 gene mutation, increase susceptibility, underscoring the need for flu vaccination.
Area of Science:
- Neurology
- Infectious Diseases
- Genetics
Background:
- Influenza A can lead to severe neurological complications in children.
- Acute necrotising encephalopathy (ANE) is a rare but devastating consequence of influenza infection.
- Genetic predispositions can increase the risk of developing ANE.
Observation:
- A 3-year-old girl presented with encephalopathy and hemiparesis due to influenza A.
- Brain MRI revealed extensive necrotic and hemorrhagic changes consistent with ANE.
- Genetic testing identified a RANBP2 gene mutation, a known risk factor for ANE.
Findings:
- The patient received prompt treatment with antivirals and corticosteroids.
- Intensive rehabilitation led to a remarkable recovery.
- The case confirms the link between influenza A, RANBP2 mutation, and ANE.
Implications:
- Highlights ANE as a severe, albeit rare, complication of influenza in children.
- Emphasizes the role of genetic factors, such as RANBP2 mutations, in ANE susceptibility.
- Stresses the importance of pediatric influenza vaccination to prevent severe outcomes.
Abstract:
We describe a case of a 3-year-old girl who was admitted with encephalopathy and a right-sided hemiparesis secondary to acute influenza A. She was up-to-date with the Australian National Immunisation Program (which does not routinely include the seasonal influenza vaccine). After initial treatment with intravenous antimicrobials and acyclovir, a brain and spinal cord MRI demonstrated extensive focal necrotic and haemorrhagic changes in keeping with acute necrotising encephalopathy (ANE). She was started on a course of oseltamivir and intravenous pulse methylprednisolone, followed by an oral weaning regimen of prednisolone. After an intense period of rehabilitation, she has made a remarkable recovery. Genetic testing has since confirmed that this girl has the RANBP2 gene mutation, which leads to increased susceptibility of developing ANE. This case report highlights ANE as a rare but severe complication of influenza, the unfortunate complication of having the RANBP2 mutation and the importance of paediatric influenza vaccination.
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