Please use this identifier to cite or link to this item:
Title: Severe optic neuritis in a patient with combined neuromyelitis optica spectrum disease and primary Sjögren's syndrome: A case report
Authors: Tan, P
Yu, W.Y 
Umapathi, T
Lim, S.-A
Keywords: antinuclear antibody
aquaporin 4 antibody
immunoglobulin G
immunoglobulin G antibody
rheumatoid factor
case report
disease severity
dry eye
immunosuppressive treatment
myelooptic neuropathy
optic disk
optic neuritis
priority journal
Sjoegren syndrome
visual acuity
visual impairment
Issue Date: 2012
Citation: Tan, P, Yu, W.Y, Umapathi, T, Lim, S.-A (2012). Severe optic neuritis in a patient with combined neuromyelitis optica spectrum disease and primary Sjögren's syndrome: A case report. Journal of Medical Case Reports 6 : 401. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: Introduction. Optic neuritis, although uncommon, can be the initial presentation of Sjögren's syndrome. Coexisting Sjögren's syndrome has also been reported with neuromyelitis optica spectrum disorder. This case report highlights the association between the two diseases and the importance of rheumatological and neurological evaluations in patients with such diagnoses. Distinction of neuromyelitis optica with coexisting connective tissue disease has both prognostic and therapeutic significance for the patient. Case presentation. We report a case of a 56-year-old Chinese woman who presented with bilateral asymmetric visual loss secondary to optic neuritis. She was subsequently found to be seropositive for neuromyelitis optica immunoglobulin G (NMO-IgG) (anti-aquaporin-4 antibody) and was diagnosed with neuromyelitis optica spectrum disorder. She also fulfilled the international criteria for Sjögren's syndrome. Despite initial high dose immunosuppressive therapy, she failed to regain vision in one eye. Conclusion: Patients presenting with optic neuritis and severe visual loss should be screened for neuromyelitis optica and treated appropriately. Neuromyelitis optica has been associated with systemic autoimmune diseases, in particular Sjögren's syndrome, and current evidence indicates that they are two distinct entities. We recommend that both diagnoses be considered in cases of optic neuritis with severe visual loss. © 2012 Tan et al.; licensee BioMed Central Ltd.
Source Title: Journal of Medical Case Reports
ISSN: 17521947
DOI: 10.1186/1752-1947-6-401
Rights: Attribution 4.0 International
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1186_1752-1947-6-401.pdf413.64 kBAdobe PDF




checked on Apr 12, 2021

Page view(s)

checked on Apr 8, 2021

Google ScholarTM



This item is licensed under a Creative Commons License Creative Commons