Please use this identifier to cite or link to this item: https://doi.org/10.1186/1752-1947-6-401
DC FieldValue
dc.titleSevere optic neuritis in a patient with combined neuromyelitis optica spectrum disease and primary Sjögren's syndrome: A case report
dc.contributor.authorTan, P
dc.contributor.authorYu, W.Y
dc.contributor.authorUmapathi, T
dc.contributor.authorLim, S.-A
dc.date.accessioned2020-10-28T07:28:11Z
dc.date.available2020-10-28T07:28:11Z
dc.date.issued2012
dc.identifier.citationTan, 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. https://doi.org/10.1186/1752-1947-6-401
dc.identifier.issn17521947
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181840
dc.description.abstractIntroduction. 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectantinuclear antibody
dc.subjectaquaporin 4 antibody
dc.subjectimmunoglobulin G
dc.subjectimmunoglobulin G antibody
dc.subjectmethylprednisolone
dc.subjectrheumatoid factor
dc.subjectadult
dc.subjectarticle
dc.subjectcase report
dc.subjectdisease severity
dc.subjectdry eye
dc.subjectfemale
dc.subjecthuman
dc.subjectimmunosuppressive treatment
dc.subjectmyelooptic neuropathy
dc.subjectneuroimaging
dc.subjectoptic disk
dc.subjectoptic neuritis
dc.subjectplasmapheresis
dc.subjectpriority journal
dc.subjectprognosis
dc.subjectSjoegren syndrome
dc.subjectvisual acuity
dc.subjectvisual impairment
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/1752-1947-6-401
dc.description.sourcetitleJournal of Medical Case Reports
dc.description.volume6
dc.description.page401
Appears in Collections:Staff Publications
Elements

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

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons