Abstract
A 49-year-old previously healthy woman presented with acute painless visual loss in the right eye, a right relative afferent pupillary defect, and a normal fundus examination. She was diagnosed with retrobulbar “optic neuritis” and given a course of intravenous steroids. Despite treatment, however, she continued to lose vision and serial visual field testing confirmed a junctional scotoma in the fellow eye. Cranial magnetic resonance imaging (MRI) showed a mass at the junction between the right optic nerve and the anterior aspect of the chiasm and a right frontal lesion that proved to be multicentric glioblastoma multiforme. Clinicians should be aware of the possibility of aggressive neoplasm in the differential diagnosis of retrobulbar optic neuritis.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 112-116 |
| Number of pages | 5 |
| Journal | Neuro-Ophthalmology |
| Volume | 42 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 4 2018 |
Keywords
- Glioblastoma multiforme
- malignant optic nerve glioma of the adult
- optic nerve tumour
- optic neuritis
ASJC Scopus subject areas
- Ophthalmology
- Clinical Neurology
Fingerprint
Dive into the research topics of 'Multicentric Glioblastoma Multiforme Mimicking Optic Neuritis'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS