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Arch Rheumatol. 2019 Nov 06;35(1):142-145. doi: 10.5606/ArchRheumatol.2020.7377. eCollection 2020 Mar.

A Rare Cause of Hypopyon Anterior Uveitis: Relapsing Polychondritis.

Archives of rheumatology

Nilüfer Zorlutuna Kaymak, Murat Oklar, Burak Tanyildiz, Mehmet Engin Tezcan, Şaban ŞİmŞek

Affiliations

  1. Department of Ophthalmology, Medical Health Sciences University, Kartal Dr. Lütfi K?rdar Training and Research Hospital, Istanbul, Turkey.
  2. Department of Rheumatology, Medical Health Sciences University, Kartal Dr. Lütfi K?rdar Training And Research Hospital, Istanbul, Turkey.

PMID: 32637931 PMCID: PMC7322311 DOI: 10.5606/ArchRheumatol.2020.7377

Abstract

Relapsing polychondritis (RP) is a rare multisystemic disease. It affects cartilage and proteoglycan-rich structures. Ocular findings are the most frequent systemic involvement of the disease. The most common ocular manifestations are episcleritis and scleritis. During the course of the disease, uveitis may also be seen. However, as far as we know, nongranulomatous anterior uveitis with hypopyon is an uncommon ocular finding. In this article, we report a 27-year-old male patient who presented with hypopyon anterior uveitis as a revealing manifestation of RP.

Copyright © 2020, Turkish League Against Rheumatism.

Keywords: Hypopyon uveitis; ocular manifestations; relapsing polychondritis

Conflict of interest statement

Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

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