Homonymous field defect as the first manifestation of Creutzfeldt-Jakob disease

Am J Ophthalmol. 1995 Apr;119(4):497-504. doi: 10.1016/s0002-9394(14)71237-1.

Abstract

Purpose: Although in the early stage of Creutzfeldt-Jakob disease most patients have obvious dementia, we found that the disease can be diagnosed in patients solely on the basis of a visual system disorder.

Methods: We examined three patients who initially complained of a nonspecific, insidious visual disturbance.

Results: The three patients were found to have Creutzfeldt-Jakob disease, confirmed by histopathologic analysis. Each patient had a homonymous hemianopsia on the first neuro-ophthalmologic examination. The initial neurologic, neuroimaging, and electrophysiologic examinations were not conclusive. The subsequent rapid deterioration in the neurologic status, including dementia and typical electroencephalographic changes, was suggestive of Creutzfeldt-Jakob disease.

Conclusion: At onset of Creutzfeldt-Jakob disease, patients may have a homonymous hemianopsia despite normal results of magnetic resonance imaging of the brain and neurologic examination.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Biopsy
  • Brain / pathology
  • Creutzfeldt-Jakob Syndrome / complications
  • Creutzfeldt-Jakob Syndrome / diagnosis*
  • Electroencephalography
  • Hemianopsia / diagnosis*
  • Hemianopsia / etiology
  • Humans
  • Male
  • Middle Aged
  • Visual Field Tests
  • Visual Fields*