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斯特奇-韦伯综合征中的青光眼和脉络膜出血机制

Glaucoma and expulsive hemorrhage mechanisms in the Sturge-Weber syndrome.

作者信息

Christensen G R, Records R E

出版信息

Ophthalmology. 1979 Jul;86(7):1360-6. doi: 10.1016/s0161-6420(79)35391-x.

Abstract

An eye from an adult with Sturge-Weber syndrome and glaucoma is described histologically following enucleation for massive choroidal hemorrhage. The specimen is noted to contain hemangiomas of the episclera and choroid as well as a partial angle cleavage abnormality. Histologic evidence reviewed herein supports the concept that infantile glaucoma associated with this syndrome may be associated with marked filtration angle cleavage deformities. Some Sturge-Weber patients who develop unilateral glaucoma later as juveniles or adults appear to have milder expressions of angle cleavage abnormality or a forme fruste of this angle disorder. Any surgical procedure for this glaucoma preferably should be one which minimizes or eliminates operative hypotony, thus avoiding a possible expulsive hemorrhage.

摘要

本文描述了一例患有斯特奇-韦伯综合征和青光眼的成年人眼球组织学情况,该眼球因大量脉络膜出血而被摘除。标本显示含有巩膜表层和脉络膜血管瘤以及部分房角劈裂异常。本文回顾的组织学证据支持这样的观点,即与该综合征相关的婴儿型青光眼可能与明显的滤过角劈裂畸形有关。一些斯特奇-韦伯综合征患者在青少年或成年期后期发生单侧青光眼,似乎有较轻的房角劈裂异常表现或这种房角疾病的顿挫型。针对这种青光眼的任何手术方法最好应能尽量减少或消除手术性低眼压,从而避免可能的驱逐性出血。

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