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绝大多数Sturge-Weber综合征仅发生单侧青光眼。作者介绍一例罕见的双侧颜面血管瘤、双侧青光眼及一侧脑部病变同时发生的Sturge-Weber综合征。病例报告:出生一天的男性新生儿,足月顺产。双侧颜面沿三叉神经分布区域及鼻、颊部粘膜均发现血管瘤,双角膜混浊,眼底未能看清,诊断为具有双侧青光眼的Sturge-Weber综合征。滴用2%匹罗卡品,口服乙酰唑胺62.5mg,每日4次,角膜仍未清亮。3周时手术治疗,右眼压为24mmHg,左眼为21mmHg。行右眼前房角切开术,术后双眼角膜仍混浊。5周时复诊,双眼角膜雾状混浊,双眼
Most unilateral glaucoma occurs in most Sturge-Weber syndromes. The authors present a case of a rare case of Sturge-Weber syndrome with bilateral hemangiomas, bilateral glaucoma, and one-sided brain lesions. Case Reports: Male Newborn One Day Birth, Full-term Birth. Bilateral facial along the trigeminal nerve distribution area and nasal, buccal mucosa were found hemangioma, double corneal opacity, fundus failed to see, diagnosed with bilateral glaucoma Sturge-Weber syndrome. Drops with 2% pilocarpine, oral acetazolamide 62.5mg, 4 times a day, the cornea is still not clear. Surgical treatment was performed at 3 weeks with a right eye pressure of 24 mmHg and a left eye of 21 mmHg. Line right anterior chamber incision, postoperative corneal opacity is still. 5 weeks referral, both eyes corneal opacity, eyes