Indian Journal of Inflammation Research

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Ocular lesions in systemic lupus erythematosus: An overview

Authors

  • Unnathi Nallagula Department of Uvea, Sankara Nethralaya, Nungambakkam, Chennai, Tamil Nadu, India
  • Ranju Kharel Department of Ophthalmology, Maharajgunj Medical College, Tribhuvan University, Institute of Medicine, Nepal, India
  • Jyotirmay Biswas Department of Uveitis & Ocular Pathology, Sankara Nethralaya, Nungambakkam, Chennai, Tamil Nadu, India

Keywords:

Systemic lupus erythematosus, SLE, ocular lesions, manifestations, retinopathy

Abstract

Systemic lupus erythematosus (SLE) is a life-threatening, multisystemic, chronic autoimmune disease. Ocular manifestations of SLE are diverse, affecting any part of the eye. It is a potentially blinding disease with ocular manifestations as the presenting feature. The prevalence of retinal involvement is estimated to be 3% to 29% and it tends to be bilateral and asymmetrical. Retinal signs often concur with the severity of systemic inflammation. Microangiopathy in SLE mimics diabetic and hypertensive retinopathy, moderately severe SLE can have presentation that mimic Purtscher-like retinopathy with a prevalence of 0.14%. Vaso-occlusive disease can either have isolated/combined, retinal artery or vein occlusion. Associated antiphospholipid antibody also increases the risk of vaso-occlusion.  The occurrence of optic neuritis and ischemic optic neuropathy is rare in SLE. Presence of peripheral ulcerative keratitis, and scleral, orbital, retinal, choroidal, and neurological manifestations require immediate systemic therapy. Hydroxychloroquine >6.5 mg/kg for 5 years is associated with high risk of toxicity. Modern imaging techniques like fluorescein angiography (FA), indocyanine green angiography (ICGA), optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) help in diagnosis and monitoring of disease activity.

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2022-06-08

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