Recurrent Anterior Uveitis with Hypopyon Revealing Relapsing Polychondritis
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概要
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Relapsing polychondritis (RP) is a rare disease involving cartilaginous structures, predominantly the ears, nose and laryngotracheobronchial tree. The eyes, cardiovascular system, peripheral joints, skin, and central nervous system may also be affected. Involvement of all ocular structures has been described. Non-granulomatous uveitis is a common feature; however hypopyon is uncommon. We herein present the case of a 42-year-old man who had been diagnosed with bronchial asthma for a long period; and who presented with recurrent hypopyon uveitis as a revealing manifestation of relapsing polychondritis. We emphasize that RP should therefore be considered in the differential diagnosis of sterile hypopyon uveitis.
著者
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Ben Salah
Department of Internal Medicine, Hedi Chaker Hospital, Tunisia
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Frikha Faten
Department of Internal Medicine, Hedi Chaker Hospital, Tunisia
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Hentati Yosr
Department of Radiology, Hedi Chaker Hospital, Tunisia
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Kallel Souha
Department of Otorhinolaryngology, Habib Bourguiba Hospital, Tunisia
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Ghorbel Abdelmoneem
Department of Otorhinolaryngology, Habib Bourguiba Hospital, Tunisia
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Mnif Zeineb
Department of Radiology, Hedi Chaker Hospital, Tunisia
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Bahloul Zouhir
Department of Internal Medicine, Hedi Chaker Hospital, Tunisia
関連論文
- Recurrent Anterior Uveitis with Hypopyon Revealing Relapsing Polychondritis
- Intracardiac Thrombus in a Young Man: Don't Forget Behçet's Disease!