Journal of Neurology and Psychology
Case Report
Aquaporin-4 Protein Antibody Seropositivity after Acute SARS-CoV-2 Infection
Tan Y1*, Zuberi HZ2, Hernandez RM1 and Avila M1
1Department of Neurology, Texas Tech University Health Sciences
Center, Lubbock, Texas
2Texas Tech University Health Sciences Center School of Medicine,
Lubbock, Texas
*Address for Correspondence:
Tan Y, Department of Neurology, Texas Tech University Health Sciences
Center, Lubbock 79430, Texas; Telephone: 806.743.2391; E-mail:
Yuanyuan.Tan@ttuhsc.edu
Submission: August 16, 2022
Accepted: September 09, 2022
Published: September 12, 2022
Copyright: © 2022 Tan Y, et al. This is an open access article distributed
under the Creative Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in any medium, provided
the original work is properly cited.
Abstract
Background: Development of autoimmune neurological disorders
after Coronavirus Disease 2019 (COVID-19) has been reported. Though
many cases of multiple sclerosis developing after COVID-19 are
present in current literature, Neuromyelitis Optica Spectrum Disorder
(NMOSD) is much rarer sequela of the disease.
Methods: Two cases that meet the international consensus
diagnostic criteria for NMOSD were encountered at a regional hospital
in West Texas in the same month. Both were preceded by acute
SARS-CoV-2 infection and developed newly diagnosed NMOSD with
Aquaporin-4 Protein Antibody seropositivity.
Results: Case 1 was a 28-year-old Hispanic female who presented
with opsoclonus and ophthalmoplegia; Case 2 was a 20-year-old
African American female who presented with transverse myelitis. Both
patients had no neurological co morbidities or symptoms prior to SARSCoV-
2 infection. Neither of them was vaccinated for COVID-19, and
both were of non-Caucasian ethnicity. They presented with a typical
features including younger onset, ocular presentation of opsoclonus,
negative neuroimaging, no response to steroids, and relapse after a
short interval.
Conclusion: New developments of NMOSD in previously healthy
individuals can be a neurological sequela of COVID-19, especially
among unvaccinated individuals. The correlation and pathophysiology
of NMOSD after COVID-19 are not fully understood, but molecular
mimicry of the virus and cytokine storm are postulated mechanisms.
Additional observational studies are needed to further explore the
correlation between acute COVID-19 infection and NMOSD.