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Sturge-Weber 氏综合征(SWS)又称脑—眼—三叉神经血管瘤病,最初于1860年Shirmer 对一例伴面血管痣的青光眼进行了报道。后由Sturge(1879年)及Weber(1922年)进一步总结。SWS 合并青光眼较复杂,多为单侧发病,手术效果差,并发症多。本文结合1例双侧SWS 先天性青光眼,术后继发闭角型青光眼,报告如下。患儿5岁男1992年6月第三次入院。父母及本人均无特殊病史。出生时双面部有片状血管痣。生后6个月时,双角膜大,眼压高。常规给予2%匹罗卡品及0.5%噻吗心安点眼,眼压波动于2.3—4.9kPa(17.30—37.19mmHg)。2岁半时,右眼眼压(4.8kPa35.76mmHg),左眼4.4kPa(32.97mmHg)。双眼交替性外斜视15°。双角膜直径14mm。结膜及巩
Sturge-Weber’s syndrome (SWS), also known as brain-eye-trigeminal hemangiomatosis, was first reported by Shirmer in 1860 as a glaucoma with vascular nevi. Later by Sturge (1879) and Weber (1922) to further summarize. SWS complicated with glaucoma, mostly unilateral disease, poor surgical results, complications and more. In this paper, a case of bilateral SWS congenital glaucoma, secondary to postoperative angle-closure glaucoma, the report is as follows. Children with 5-year-old boy in June 1992 the third admission. Parents and I have no special medical history. Duplex at birth have flake nevus. 6 months after birth, double cornea, high intraocular pressure. Conventional given 2% pilocarpine and 0.5% timolol eye, intraocular pressure fluctuations in the 2.3-4.9kPa (17.30-37.19mmHg). Two and a half years old, the right eye intraocular pressure (4.8kPa35.76mmHg), left eye 4.4kPa (32.97mmHg). Eyes alternating exotropia 15 °. Double corneal diameter 14mm. Conjunctival and Gong