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Clinical characteristics of Vogt-Koyanagi-Harada disease in two elderly persons Noriyoshi Ichigashira 1 , Masahiko Kozawa 1 , Midori Noda 1 , Kohji Murata 1 , Hideyuki Hayashi 1 , Eiichi Uchio 1 1Dept of Ophthalmol, Fukuoka Univ Sch of Med pp.493-497
Published Date 2008/4/15
DOI https://doi.org/10.11477/mf.1410102194
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Abstract. Background:Vogt-Koyanagi-Harada(VKH)disease is claimed to mainly affect persons in the third to fifth decade of life. When it occurs in persons in advanced age, difficulties may arise to distinguish the characteristic skin and extraocular manifestations of the disease from age-related physiological changes. Due attention is required with the use of systemic corticosteroid regarding systemic side effects in the elderly. Purpose:To report two cases of VKH disease in elderly persons. Cases:We diagnosed a 83-year-old female and a 60-year-old male with VKH disease. The first case had had ear pain and difficulty in hearing since 4 weeks. She noted ocular pain and blurring 4 days before. Her corrected visual acuity was 0.6 right and 0.4 left. Her left eye showed signs of iritis. Both eyes showed hyperemia and swelling of the optic disc with retinal detachment in the papillomacular area. Cerebrospinal fluid showed pleocytosis. The other case presented with 2 weeks after onset of blurring in both eyes. Visual acuity was 0.15 right and 0.2 left. Both eyes showed keratitic precipitates, disc edema and retinal detachment in the papillomacular area. Pleocytosis was present in the cerebrospinal fluid. Both cases were positive for DR4 by HLA typing. Pulsed corticosteroid was followed by improvement in both cases. Conclusion:VKH in the two aged persons responded well to systemic corticosteroid. HLA typing and cerebrospinal tap was useful in the diagnosis.


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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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