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.
Abstract