Vogt-Koyanagi-Harada syndrome presenting as bilateral simultaneous acute angle closure

Swati Singh, S. Kaushik, Savleen Kaur, Ramandeep Singh, S. Pandav
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引用次数: 2

Abstract

Presentation of bilateral simultaneous angle closure in a patient must alert one to look beyond the common “knee-jerk” diagnosis of acute primary angle closure (APAC). We describe a case with bilateral simultaneous acute angle closure with signs of anterior chamber inflammation with intraocular pressure of 60 mmHg. Based on the clinical details and ultrasonic findings of peripapillary choroidal thickening and supraciliary fluid, a diagnosis of Vogt-Koyanagi-Harada (VKH) disease was made. Our case highlights that every angle closure is not a primary angle closure requiring laser peripheral iridotomy. Detailed clinical examination with appropriate investigations could prevent misdiagnosis of APAC in VKH.
Vogt-Koyanagi-Harada综合征表现为双侧同时急性角关闭
患者双侧同时闭角的表现必须提醒人们要超越急性原发性闭角(APAC)的常见“下意识”诊断。我们描述了一个病例,双侧同时急性闭角,有前房炎症的迹象,眼压为60 mmHg。根据临床细节和超声检查的乳头周围脉络膜增厚和睫上积液,诊断为Vogt-Koyanagi-Harada (VKH)病。我们的病例强调,并非所有闭角都是需要激光虹膜周围切开术的原发性闭角。详细的临床检查和适当的调查可以防止APAC在VKH中的误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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