一名11岁男孩的Vogt-小柳-原田综合征
Vogt-Koyanagi-Harada syndrome in an 11-year-old Boy.
作者信息
Ikeda N, Hayasaka S, Kadoi C, Nagaki Y
机构信息
Department of Ophthalmology, Toyama Medical and Pharmaceutical University, Toyama, Japan.
出版信息
Ophthalmologica. 1999;213(3):197-9. doi: 10.1159/000027419.
An 11-year-old boy complained of headache, slight fever and decreased visual acuity. Intracameral cells and serous retinal detachment were found in both eyes. Pleocytosis was seen in the cerebrospinal fluid. Bilateral uveitis diminished rapidly in response to corticosteroid treatment. Depigmentation of the fundi developed several months later. We believe that Vogt-Koyanagi-Harada syndrome in a child, as demonstrated in our patient, may be uncommon.
一名11岁男孩主诉头痛、低热及视力下降。双眼前房内有细胞及浆液性视网膜脱离。脑脊液中可见细胞增多。双侧葡萄膜炎对皮质类固醇治疗反应迅速消退。数月后眼底出现色素脱失。我们认为，如我们的患者所示，儿童Vogt-小柳-原田综合征可能并不常见。
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