Journals / Retina-Vitreus / 2012 / Cilt: 20 - Sayı: 3

Yaygın koryoretinitli bir subakut sklerozan panensefalit olgusu

A case of subacute sclerosing panencephalitis with widespread chorioretinitis

Pages
230–232
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

SSPE should be considered in the differential diagnosis of optic atrophy and atypical widespread chorioretinitis in young patients, especially in countries where SSPE has a higher incidence rate.

📌 3 Key Takeaways

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Objective & Hypothesis:The purpose of this study was to report a SSPE patient presenting with bilateral optic atrophy, maculopathy, and widespread chorioretinitis.
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Key Findings & Data:A 14-year-old girl was admitted to our hospital with the complaint of sudden painless visual loss in both eyes with a 1-month interval.
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Conclusion & Impact:SSPE should be considered in the differential diagnosis of optic atrophy and atypical widespread chorioretinitis in young patients, especially in countries where SSPE has a higher incidence rate.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The purpose of this study was to report a SSPE patient presenting with bilateral optic atrophy, maculopathy, and widespread chorioretinitis. A 14-year-old girl was admitted to our hospital with the complaint of sudden painless visual loss in both eyes with a 1-month interval. Best corrected visual acuity was finger counting level in both eyes. Bilateral optic atrophy, macular scar, and chorioretinitis affecting the whole posterior segment were observed. Encephalopathy and convulsions developed 2 months after the presentation of eye findings. She was diagnosed with SSPE according to clinical, electroencephalographic, and cerebrospinal fluid findings. SSPE should be considered in the differential diagnosis of optic atrophy and atypical widespread chorioretinitis in young patients, especially in countries where SSPE has a higher incidence rate.

Özet

Bu çalışmanın amacı, her iki gözde optik atrofi, makülopati ve yaygın koryoretinit bulgularıyla başlayan bir SSPE olgusunu sunmaktır. On dört yaşında bayan hasta, her iki gözde bir ay ara ile gelişen, ağrısız ani görme kaybı şikayeti ile hastanemize başvurdu. Düzeltilmiş uzak görme keskinliği her iki gözde el hareketlerini seviyesindeydi. Arka segmet muayenesinde, her iki gözde optik atrofi, makülada skar ve tüm arka kutbu etkilemiş koryoretinit bulguları izlendi. 2 ay sonra hastada konvulsiyonlar ve ensefalopati tablosu gelişti. Klinik tablo, elektroensefalografik değerlendirme ve beyin omurilik sıvısının incelenmesi sonucunda elde edilen bulgularla hastaya SSPE tanısı kondu. Özellikle SSPE insidansının daha yüksek olduğu ülkelerde, optik atrofi ve atipik yaygın koryoretinit izlenen genç hastalarda, SSPE tanısı akılda tutulmalıdır.

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Cite This Article

UĞURLU, N., ÇAĞIL, N., ARHAN, E., KÖSE, G., ŞENGÜN, A. (2012). Yaygın koryoretinitli bir subakut sklerozan panensefalit olgusu. Retina-Vitreus, Cilt: 20 - Sayı: 3, 230–232. https://ajindex.com/articles/308071

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