Retinal vasculitis – Current approach to diagnosis, investigations, and management

Retinal vasculitis is defined as the inflammation of the retinal vessel wall, which may involve the veins (periphlebitis), arteries (periarteritis), capillaries (capillaritis), or a combination of these. It is an uncommon sight-threatening retinal vascular inflammatory disorder resulting in a plethora of clinical features. It may be associated with systemic inflammatory conditions, infections, neoplastic diseases, or may be idiopathic. Reaching a diagnostic etiology for retinal vasculitis is often a diagnostic challenge. Meticulous examination, essential laboratory investigations, fundus photography, autofluorescence, fundus fluorescein angiography, indocyanine green angiography, optical coherence tomography (OCT), OCT angiography, B scan ultrasonography, and widefield fundus imaging enable us to arrive at a diagnosis. Antivascular endothelial growth factor and laser photocoagulation help to arrest neovascularization. Newer agents, such as immunomodulators and biologics, are effective against these sight-threatening conditions. Early management often helps to salvage vision and minimize comorbidities in these conditions. This review highlights on diagnosis and management of retinal vasculitis.

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Publication Details

Journal
Journal of Ophthalmic Research and Practice
Published
2024-11-23
DOI
https://doi.org/10.25259/jorp_34_2024
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
Field-Weighted Citation Impact
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article

Retinal vasculitis – Current approach to diagnosis, investigations, and management

Jyotirmay Biswas, Namitha Rachel Mathew
Journal of Ophthalmic Research and Practice
Ocular Diseases and Behçet’s Syndrome
article

Retinal vasculitis – Current approach to diagnosis, investigations, and management

Jyotirmay Biswas, Namitha Rachel Mathew
article en

Abstract

Retinal vasculitis is defined as the inflammation of the retinal vessel wall, which may involve the veins (periphlebitis), arteries (periarteritis), capillaries (capillaritis), or a combination of these. It is an uncommon sight-threatening retinal vascular inflammatory disorder resulting in a plethora of clinical features. It may be associated with systemic inflammatory conditions, infections, neoplastic diseases, or may be idiopathic. Reaching a diagnostic etiology for retinal vasculitis is often a diagnostic challenge. Meticulous examination, essential laboratory investigations, fundus photography, autofluorescence, fundus fluorescein angiography, indocyanine green angiography, optical coherence tomography (OCT), OCT angiography, B scan ultrasonography, and widefield fundus imaging enable us to arrive at a diagnosis. Antivascular endothelial growth factor and laser photocoagulation help to arrest neovascularization. Newer agents, such as immunomodulators and biologics, are effective against these sight-threatening conditions. Early management often helps to salvage vision and minimize comorbidities in these conditions. This review highlights on diagnosis and management of retinal vasculitis.

Journal of Ophthalmic Research and PracticeVol. 2
Sankara Nethralaya (IN)
Openalex Percentile: Top 66%
Ocular Diseases and Behçet’s Syndrome
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