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eISSN: 2719-3209
ISSN: 0023-2157
Klinika Oczna / Acta Ophthalmologica Polonica
Bieżący numer Archiwum Filmy Artykuły w druku O czasopiśmie Suplementy Rada naukowa Bazy indeksacyjne Prenumerata Kontakt Zasady publikacji prac Standardy etyczne i procedury
3/2020
vol. 122
 
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Opis przypadku

Vogt-Koyanagi-Harada disease – a rare entity in the Polish population – a case report

Martyna Słomska
1
,
Julia Kręcicka
1
,
Radosław Kaczmarek
1
,
Anna Turno-Kręcicka
1

1.
Department and Clinic of Ophthalmology, University Clinical Hospital in Wroclaw, Poland
KLINIKA OCZNA 2020, 122, 3: 128–134
Data publikacji online: 2020/07/23
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Vogt-Koyanagi-Harada (VKH) disease is an idiopathic autoimmune reaction against tissues containing melanocytes. Typical eye symptoms are bilateral granulomatous panuveitis and serous retinal detachment (SRD). At a later stage it leads to extensive depigmentation of the fundus (“sunset glow fundus”). The symptoms are accompanied by neurological, auditory or integumentary disorders. The diagnosis is based on clinical findings. In this article we present a case of a 39-year-old man, who had been mistakenly treated for many months before the correct diagnosis was made. Our research is one of the first publications describing Vogt-Koyanagi-Harada disease in the Polish population; therefore this diagnosis is rarely considered.
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