PURPOSE:To determine the applicability of the international revised diagnostic criteria for Vogt-Koyanagi-Harada disease. METHODS:Retrospective study. Medical charts of 140 patients with the diagnosis of Vogt-Koyanagi-Harada disease, from the Uveitis Sector of the Federal University of Sao Paulo (UNIFESP), were revised and classified following the revised diagnostic criteria. RESULTS:Of the 140 patients, 12.85% fulfilled the criteria for complete disease, 29.28% incomplete disease, 28.57% "probable" Vogt-Koyanagi-Harada disease and 28.27% were considered not Vogt-Koyanagi-Harada disease. CONCLUSION:The authors consider that the international revised diagnostic criteria have good applicability and are very useful to help in the diagnosis of Vogt-Koyanagi-Harada disease.

译文

目的:确定国际修订的沃格特-小柳-原田病诊断标准的适用性。
方法:回顾性研究。根据修订后的诊断标准,对来自圣保罗联邦大学葡萄膜炎科的140名诊断为Vogt-Koyanagi-Harada病的患者的病历表进行了修订和分类。
结果:140例患者中,完全性疾病的标准为12.85%,不完全性疾病的标准为29.28%,“可能”沃格特-小柳原田病的患病率为28.57%,被认为不是沃格特-小柳原田原病的28.27%。
结论:作者认为,国际修订的诊断标准具有良好的适用性,对于帮助诊断Vogt-Koyanagi-Harada病非常有用。

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