A Case of Behçet’s Uveitis – A Delay in the Diagnosis

Published

2026-04-02

DOI:

https://doi.org/10.56692/upjo.2026140110

Keywords:

Behçet’s, Vitritis, HLAB51 positive, Tofacitinib

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Authors

  • Shravan Subramanian JR-2, Netrodaya The Eye City, Varanasi, Uttar Pradesh, India
  • Soumya Ray VR Fellow, Netrodaya The Eye City, Varanasi, Uttar Pradesh, India
  • Abhishek Chandra Consultant Netrodaya The Eye City
  • Neha Shilpy Consultant Netrodaya The Eye City

Abstract

Behçet’s uveitis is a severe ocular manifestation of Behçet’s disease, a chronic, relapsing multisystem vasculitis. It typically presents as bilateral, recurrent, non-granulomatous panuveitis with occlusive retinal vasculitis involving both arteries and veins. Common ocular signs include hypopyon, hemorrhages, vitritis and retinal infiltrates. The underlying pathogenesis involves immune dysregulation in genetically predisposed individuals, often associated with HLA-B51.

How to Cite

1.
Subramanian S, Ray S, Chandra A, Shilpy N. A Case of Behçet’s Uveitis – A Delay in the Diagnosis. UPJO [Internet]. 2026 Apr. 2 [cited 2026 Jun. 26];14(01):44-5. Available from: https://upjo.info/index.php/upjo/article/view/635

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