| Literature DB >> 31988053 |
Tiago Gama Ramires1,2, Luísa Vieira3, Nuno Riso4, Maria Francisca Moraes-Fontes2.
Abstract
A 23-year-old woman with fever, oral ulcers, arthalgias and weight loss of 2-week duration suddenly developed blurred vision, with reduced visual acuity, cotton wool exudates and retinal vascular tortuosity. Laboratory testing revealed anaemia, lymphopaenia, positive antinuclear antibody and high anti-dsDNA antibody titre with low complement components. There was no evidence of infection, clinching the diagnosis of lupus retinopathy. Steroid therapy alone was highly effective and was also accompanied by a normalisation of haemoglobin and lymphocyte counts, after which azathioprine was added. Hydroxychloroquine was introduced after resolution of retinal changes. Immunosuppressive therapy was progressively tapered over the course of 12 months and then discontinued, and the patient remains in remission 48 months after the initial presentation. Our patient exemplifies a very rare manifestation of systemic lupus erythematosus. We emphasise the importance of its early detection and complexity of treatment in order to reduce visual morbidity. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: immunology; retina; systemic lupus erythematosus
Mesh:
Year: 2020 PMID: 31988053 PMCID: PMC7021184 DOI: 10.1136/bcr-2019-229382
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X