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Complete bilateral ophthalmoplegia in malignant intracranial hypertension in a child
Emanuela Interlandi1, Francesco Pellegrini2, Marco De Luca1
1Department of Ophthalmology, "Ospedale del Mare", ASL Napoli 1-Centro, Naples, Campania, Italy.
Insights
This case report details a rare, severe presentation of idiopathic intracranial hypertension (IIH) in a child, characterized by sudden vision loss and paralysis of eye movements without headache.
Area of Science:
- Ophthalmology
- Neurology
- Pediatrics
Background:
- Idiopathic intracranial hypertension (IIH) typically presents with headache, visual disturbances, and papilledema.
- Fulminant or "malignant" presentations of IIH are rare, especially in pediatric cases.
Purpose of the Study:
- To document a unique case of fulminant idiopathic intracranial hypertension (IIH) in a pediatric patient.
- To highlight a severe, atypical presentation of IIH with profound visual loss and ophthalmoplegia.
Main Methods:
- Case report of a 16-year-old female with acute bilateral visual loss and ophthalmoplegia.
- Diagnostic workup included MRI and lumbar puncture to confirm IIH.
- Exclusion of infectious, inflammatory, autoimmune, and neoplastic causes.
Main Results:
- Diagnosis of IIH confirmed by elevated intracranial pressure and MRI findings.
- Patient presented with severe vision loss and complete limitation of eye movements, notably without headache.
- Optic disc edema and extraocular motility showed partial improvement, but visual acuity remained significantly impaired.
Conclusions:
- A severe, acute, and fulminant ("malignant") presentation of IIH can cause unique symptoms like complete ophthalmoplegia and severe vision loss.
- The absence of headache in this IIH case is noteworthy.
- This represents the first reported case of such a "malignant" IIH presentation in the English ophthalmic literature.
Purpose:
To describe a case of fulminant idiopathic intracranial hypertension (IIH) in a child with "malignant" presentation.
Case Report:
A 16-year-old, previously healthy, girl presented with bilateral visual loss and bilateral global limitation of eye movements in the absence of headache. Extensive laboratory evaluation for infectious, inflammatory, autoimmune, and neoplastic conditions was negative. Magnetic resonance imaging (MRI) of the brain and lumbar puncture findings were consistent with a diagnosis of IIH. Extraocular motility improved in the next few days as well as optic disc edema but visual acuity remained poor.
Conclusion:
The authors believe that the acute, severe, and fulminant ("malignant") presentation with markedly elevated intracranial pressure may produce the unique presentation of severe vision loss and bilateral complete ophthalmoplegia. Interestingly, there was no headache. To our knowledge this is the first such case to be reported in the English language ophthalmic literature.
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