A Rare Ocular Manifestation of Adult Onset Still’s Disease: Purtscher’s-like Retinopathy
Ocular Immunology and Inflammation, cilt.26, sa.2, ss.286-291, 2018 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Kısa Makale
- Cilt numarası: 26 Sayı: 2
- Basım Tarihi: 2018
- Doi Numarası: 10.1080/09273948.2016.1213857
- Dergi Adı: Ocular Immunology and Inflammation
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.286-291
- Anahtar Kelimeler: Adult-onset Still's disease, corticosteroids, microangiopathy, Purtscher's-like retinopathy, Yamaguchi
- Sağlık Bilimleri Üniversitesi Adresli: Evet
Özet
Adult-onset Still’s disease (AOSD) is a rare multisystemic immune-mediated disease of unknown etiology with quotidian spiking fever, evanescent rash, arthralgia, and multiple organ involvement. The few AOSD cases that have been reported developed Purtscher’s-like retinopathy associated with thrombotic microangiopathy (TMA). Here, we report Purtscher’s-like retinopathy without TMA in a patient with AOSD. A 29-year-old-man who presented for evaluation of blurred vision was diagnosed with AOSD based on Yamaguchi criteria. He had Purtscher’s-like retinopathy in his right eye. Lesions improved after steroid treatment. Although almost all reported AOSD cases with Purtscher’s-like retinopathy are associated with TMA, in this case such a complication was not encountered.