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Outcome of Vogt-Koyanagi-Harada disease as related to clinical types Mariko Egawa 1 , Yuki Hayashi 1 , Yoshinori Mitamura 1 1Dept of Ophthalmol, Inst of Health Biosci, The Univ of Tokushima Grad Sch pp.981-984
Published Date 2013/6/15
DOI https://doi.org/10.11477/mf.1410104780
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Abstract. Purpose:To report the outcome of Vogt-Koyanagi-Harada(VKH)disease as related to the clinical types. Cases and Method:This retrospective study was made on 24 cases of VKH disease seen by us in the past 3 years. The series comprised 15 males and 9 females. The age ranged from 26 to 69 years, average 45 years. They were followed up for 9 months or longer and were evaluated regarding clinical type, degree of sunset-glow fundus, and visual function. Results:Retinal detachment in the posterior fundus was present in 16 cases. Eight cases showed peripapillary edema. The age averaged 37 and 62 years respectively. The difference was significant. Clinical manifestations resolved early in 15 cases and protracted in 9 cases. The age averaged 40 and 54 years respectively. The difference was significant. Protracted course resulted in 58% of cases with sunset-glow fundus. Cases with more advanced sunset-glow fundus showed more thinning of the choroid(p=0.01)and lower sensitivity for short-wavelength perimetry(p=0.006)than the rest. Conclusion:Visual function is more affected in cases of VKH disease that show protracted course or more manifest sunset-glow fundus.


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

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