Evidence map›Paper›PMID 42258091›Full record

ArticleJournal of ophthalmic inflammation and infection2026

A rare case of multisystem autoimmune disease presenting with retinopathy and alopecia post COVID-19 vaccination.

Srinivasan Sanjay, Samanthila Waduthantri, Manju Chandran, Soon-Phaik Chee

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Article in Journal of ophthalmic inflammation and infection, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Srinivasan SanjaySingapore National Eye Centre, 11 Third Hospital Avenue, Singapore, 168751, Singapore. sanjay.srinivasan@gmail.com.ORCID http://orcid.org/0000-0001-9756-1207
Samanthila WaduthantriSingapore National Eye Centre, 11 Third Hospital Avenue, Singapore, 168751, Singapore.ORCID http://orcid.org/0000-0001-8587-2411
Manju ChandranOsteoporosis and Bone Metabolism Unit, Department of Endocrinology, Singapore General Hospital (SGH), Life Centre (Level 4), Outram Road, Singapore, 169608, Singapore.ORCID http://orcid.org/0000-0001-9119-8443
Soon-Phaik CheeSingapore National Eye Centre, 11 Third Hospital Avenue, Singapore, 168751, Singapore.ORCID http://orcid.org/0000-0002-6308-5721

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo report a case of autoimmune retinopathy (AIR) with multiple systemic involvement

resultsA 45-year-old Asian Indian male presented with progressive blurring of vision in the right eye for five years. Initial best-corrected visual acuity (BCVA) was 20/80 in RE and 20/25 in LE. Clinical evaluation was normal except for a few pigmentary alterations in the periphery. Optical coherence tomography (OCT) later revealed ellipsoid zone loss, and fundus fluorescein angiography showed peripheral venular leakage. Uveitis workup was negative except for a positive T-spot TB; Anti-tubercular therapy for nine months didn't improve the symptoms, with BCVA declining to 20/400 in RE. Fundus autofluorescence demonstrated hypo-autofluorescence in the macula surrounded by hyper-autofluorescence. Review of history revealed dermatological features, including alopecia areata and scalp vitiligo, followed by ocular disease and systemic autoimmune abnormalities. The history also indicated onset about two months after COVID-19 vaccination. Antiretinal and other systemic antibodies were positive. The patient was diagnosed with auto immune retinopathy (AIR) and treated with mycophenolate mofetil, escalating to 1.5 g twice daily. At final follow-up 6 months later, BCVA improved to 20/200 in RE and remained stable in LE, with reduced autofluorescence abnormalities.

conclusionWe report a case of multi system autoimmune disease initially presenting with dermatological features, followed by ocular and other systemic features which may have been triggered following COVID-19 vaccination in an otherwise healthy Indian male. We propose it could be a temporal event and are unable to prove a causal factor. A combination of multimodal imaging with multi-disciplinary approach helped us to come to a final diagnosis in this arduous journey for the patient.

Indexed as

Antiretinal antibodiesAutoimmune retinopathyCOVID-19ImmunosuppressionMultimodal imagingVaccination

Identifiers

PMID42258091
PMCPMC13538326

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