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Yapay Zeka Hızlı Bakış & Çıkarımlar
AI Insight⚡ TL;DR(1 Cümlede Hızlı Çıkarım)
In this article, we report a 27-year-old male patient who presented with hypopyon anterior uveitis as a revealing manifestation of RP.
📌 3 Maddede Bu Makale
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Amaç & Hipotez:Relapsing polychondritis (RP) is a rare multisystemic disease.
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Temel Bulgular & Veri:It affects cartilage and proteoglycan-rich structures.
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Sonuç & Katkı:In this article, we report a 27-year-old male patient who presented with hypopyon anterior uveitis as a revealing manifestation of RP.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri
Özet
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.
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Bu Makaleye Atıf Yap
KAYMAK, N. Z., OKLAR, M., TANYILDIZ, B., TEZCAN, M. E., ŞİMŞEK, Ş. (2020). A Rare Cause of Hypopyon Anterior Uveitis: Relapsing Polychondritis. art, Cilt: 35 - Sayı: 1, 142–145. https://ajindex.com/articles/144407