Affiliation:
1. Department of Neurological Sciences University of Nebraska Medical Center Omaha NE USA
2. Department of Ophthalmology Stanley M. Truhlsen Eye Institute, University of Nebraska Medical Center Omaha NE USA
3. Department of Ophthalmology and Visual Sciences The Medical College of Wisconsin Milwaukee WI USA
Abstract
AbstractBackgroundSevere acute respiratory syndrome coronavirus 2 (SARSCoV2) has been associated with several neuro‐ophthalmic manifestations. We report a case of bilateral longitudinally extensive optic perineuritis suspected due to SARSCoV2.Case PresentationA 32‐year‐old woman developed headaches, photophobia, pulsatile tinnitus, and blurred vision 8 d after having a positive SARS‐CoV‐2 qualitative polymerase chain reaction (PCR) testing for coronavirus disease 2019 (COVID‐19). She was diagnosed with and treated for idiopathic intracranial hypertension (IIH) elsewhere. Repeat evaluation at our institution showed a poor visual acuity in both eyes with Frisen grade II papilledema and cotton wool spots on fundoscopic examination. Orbital magnetic resonance imaging (MRI) showed bilateral longitudinally extensive optic nerve sheath enhancement. Repeat lumbar puncture revealed an elevated cerebrospinal fluid (CSF) opening pressure and protein, a finding that is incompatible with the diagnosis of IIH. Myelin oligodendrocyte glycoprotein, aquaporin‐4 (AQP4)‐IgG antibodies, and other serological tests for optic neuritis were unremarkable. Her visual acuity partially improved after corticosteroids. With the growing association of demyelinating disorders and COVID‐19, unremarkable serological workup, and temporal relation of the patient's symptoms to the infection, we believe that her diagnosis is SARS‐CoV‐2 associated bilateral optic neuritis.ConclusionThere is a growing association between demyelinating disorders and COVID‐19 and COVID‐19 vaccination, and it is essential to recognize CSF abnormalities that are incompatible with a diagnosis of IIH, such as increased protein in our case, and may lead to an incorrect diagnosis.
Subject
Neurology (clinical),Immunology and Microbiology (miscellaneous),Immunology,Neuroscience (miscellaneous)
Cited by
3 articles.
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