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Childhood hepatitis A virus infection complicated by pseudotumor cerebri
Rajoo Thapa1, Apurba Ghosh, Swapan Mukherjee
1Department of Pediatrics and Pediatric Neurology Unit, The Institute of Child Health, Kolkata, West Bengal, India. rajoothapa@yahoo.co.in
Insights
Hepatitis A virus infection in a child led to pseudotumor cerebri, a condition causing increased intracranial pressure. This rare complication resolved spontaneously, marking the first reported pediatric case.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Ophthalmology
Background:
- Hepatitis A virus (HAV) infection is common in children.
- Pseudotumor cerebri (PC), or idiopathic intracranial hypertension, is rare in pediatric populations.
- Neurological complications of HAV are not well-documented.
Observation:
- A 4-year-old boy with HAV infection developed symptoms of increased intracranial pressure.
- Clinical signs included right sixth cranial nerve palsy.
- Cerebrospinal fluid and MRI scans were normal, consistent with PC diagnosis.
Findings:
- The patient presented with pseudotumor cerebri secondary to hepatitis A virus infection.
- Neurological examination revealed isolated sixth nerve paresis.
- Complete neurological recovery occurred spontaneously within three days.
Implications:
- This case highlights a rare neurological complication of pediatric hepatitis A.
- It suggests a potential, albeit uncommon, association between HAV and pseudotumor cerebri in children.
- Further research may elucidate the underlying mechanisms of this association.
Abstract:
A 4-year-old male child with hepatitis A virus (HAV) infection is presented. His disease course was complicated by the development of pseudotumor cerebri (PC), as evidenced by symptoms and signs of increased intracranial pressure in the presence of normal cerebrospinal fluid examination and cranial magnetic resonance scan. The neurological examination was normal with the exception of the right-sided sixth cranial nerve paresis. His neurological course was uncomplicated with spontaneous recovery within three days. To our knowledge, this is the first report in the English literature of PC complicating the course of HAV in a child.
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