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Obstructive sleep apnea syndrome with bilateral papilledema and vision loss in a 3-year-old child
Anthony G Quinn1, Pieter Gouws, Sophie Headland
1West of England Eye Unit, Royal Devon and Exeter Hospital, Exeter, United Kingdom. anthony.quinn@rdehc-tr.swest.nhs.uk
Insights
Obstructive sleep apnea can cause dangerous intracranial pressure in children, even without craniosynostosis. This condition can lead to papilledema and vision loss, highlighting the need for prompt diagnosis and management.
Area of Science:
- Pediatric Neurology
- Ophthalmology
- Sleep Medicine
Background:
- Obstructive sleep apnea (OSA) is increasingly recognized in children.
- Elevated intracranial pressure (ICP) is a serious neurological condition.
- Papilledema and vision loss are critical signs of increased ICP.
Observation:
- A 3-year-old child presented with bilateral papilledema and vision loss.
- The child had a diagnosis of obstructive sleep apnea.
- Initial lumbar puncture showed normal cerebrospinal fluid (CSF) opening pressure.
Findings:
- Continuous CSF pressure monitoring during sleep revealed intermittent ICP elevations.
- These ICP spikes correlated with increased airway resistance during sleep.
- This association was observed in the absence of craniosynostosis.
Implications:
- Obstructive sleep apnea may be an under-recognized cause of elevated intracranial pressure in children.
- This finding expands the known associations of OSA with neurological complications.
- Early recognition and management of OSA are crucial to prevent vision loss and neurological damage.
Abstract:
We describe bilateral papilledema and vision loss in a 3-year-old child with obstructive sleep apnea. Although lumbar puncture initially disclosed a normal opening pressure, cerebrospinal fluid (CSF) pressure monitoring during sleep confirmed intermittent episodes of elevated intracranial pressure corresponding to increased airway resistance. The association of obstructive sleep apnea and raised intracranial pressure is recognized in children with craniosynostosis but has not been reported in its absence.
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