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Multicentric Glioblastoma Multiforme Mimicking Optic Neuritis
Francesco Pellegrini1, Andrew G Lee2,3,4,5,6,7,8, Cristina Cercato9
1Neuro-Ophthalmology Service, Department of Ophthalmology, De Gironcoli Hospital, Conegliano, Italy.
A previously healthy woman experienced sudden vision loss, initially diagnosed as optic neuritis. Further investigation revealed a rare case of multicentric glioblastoma multiforme presenting as optic nerve and chiasm mass.
Area of Science:
- Neuro-oncology
- Ophthalmology
- Neurology
Background:
- Retrobulbar optic neuritis is an inflammatory condition affecting the optic nerve behind the eye.
- It typically presents with sudden, painless vision loss and visual field defects.
- Steroid treatment is the standard initial therapy for optic neuritis.
Observation:
- A 49-year-old woman presented with acute, painless right eye vision loss and a relative afferent pupillary defect.
- Fundus examination was normal, leading to an initial diagnosis of retrobulbar optic neuritis.
- Despite intravenous steroid treatment, her vision progressively worsened, with new visual field defects in the fellow eye.
Findings:
- Cranial magnetic resonance imaging (MRI) identified a mass at the right optic nerve-chiasm junction and a right frontal lesion.
- Biopsy confirmed the lesions to be multicentric glioblastoma multiforme, an aggressive brain tumor.
- This presentation highlights an unusual etiology for optic nerve compromise.
Implications:
- Glioblastoma multiforme can mimic inflammatory optic nerve conditions, necessitating a broad differential diagnosis.
- Clinicians should consider aggressive neoplasms in cases of atypical or treatment-refractory optic neuritis.
- Early and accurate diagnosis of CNS tumors is crucial for timely intervention and improved patient outcomes.
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