Mahendradas Padmamalini, Biswas Jyotirmay, Khetan Vikas
Department of Uveitis and Ocular Immunology, Narayana Nethralaya, Rajajinagar, Bangalore, India.
Ocul Immunol Inflamm. 2007 Nov-Dec;15(6):451-4. doi: 10.1080/09273940701798454.
To report a case of fibrinous anterior uveitis due to cysticercus cellulosae in anterior chamber.
Retrospective, interventional case study.
Patient underwent complete ophthalmic and systemic evaluation with relevant investigations. Viscoexpression of anterior chamber cysts were done under general anaesthesia.
A 10-year-old male child presented as unilateral fibrinous iridocylitis with secondary glaucoma. Two cysts of cysticercus cellulosae were seen after control of inflammation. Complete resolution of uveitis occurred once the cysts were removed by viscoexpression.
Cysticercus cellulosae can present as fibrinous anterior uveitis with secondary glaucoma. Removal of the cyst can cause complete resolution of uveitis.
报告一例因前房囊尾蚴引起的纤维素性前葡萄膜炎病例。
回顾性介入性病例研究。
患者接受了全面的眼科和全身评估及相关检查。在全身麻醉下对前房囊肿进行粘弹剂挤压术。
一名10岁男性儿童表现为单侧纤维素性虹膜睫状体炎并继发青光眼。炎症得到控制后可见两个囊尾蚴囊肿。通过粘弹剂挤压术取出囊肿后,葡萄膜炎完全消退。
囊尾蚴可表现为纤维素性前葡萄膜炎并继发青光眼。囊肿的去除可使葡萄膜炎完全消退。