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[角膜葡萄肿-前房发育不全-小眼球综合征]

[Corneal staphyloma-anterior chamber agenesia-microphakia syndrome].

作者信息

Rohrbach J M, Süsskind D, Szurman P, Siepmann K

机构信息

Universitäts-Augenklinik, Abt. I, Tübingen.

出版信息

Klin Monbl Augenheilkd. 2006 Feb;223(2):168-75. doi: 10.1055/s-2005-858732.

Abstract

CASE REPORT

Shortly after birth, a massive enlargement of the right eye was observed in an otherwise healthy male child. The cornea of the affected eye was vascularized and completely cloudy without a sharp border between cornea and sclera. The diagnosis of a congenital glaucoma was made but an operation was not undertaken because of the difficult anatomical situation and the lost function. When the child was almost 3 years old enucleation was performed to prevent complications due to corneal exposure, and to improve the cosmetic aspect.

RESULTS

The morphological investigations of the enucleated eye disclosed findings typical of what is called in the literature "congenital anterior staphyloma" or "congenital corneal staphyloma", namely a massively staphylomatous cornea with superficial neovascularization, destruction of Bowman's layer, and absence of Descemet's layer as well as corneal endothelium. Angle structures were completely absent, and the corneal back-side was lined by a pigment epithelial layer and focally by an additional inner layer of non-pigmented epithelium. There was no anterior chamber. The lens was markedly diminished in size (microphakia) and partly embedded in the corneal stroma. Pars muscularis and pars ciliaris of the ciliary body were separated. Elongated, thin ciliary processes were extended towards the small lens while the pars muscularis was fully covered by the retina.

CONCLUSIONS

This rare, complex malformation syndrome which can be easily distinguished from primary congenital glaucoma should not be reduced conceptually to the corneal staphyloma because this staphyloma constitutes only a part of the whole. Taking the leading morphological aberrations into consideration we would rather propose the new term " corneal staphyloma- anterior chamber agenesia- microphakia syndrome (CSAMS). We hypothesize that CSAMS may be due to a pathological fusion of the early anterior optic cup. As the posterior eye segment is often normal in CSAMS, a staphyloma excision along with a sclero-keratoplasty might be an alternative therapeutic option to avoid enucleation and restore ambulatory vision.

摘要

病例报告

一名原本健康的男婴出生后不久,右眼出现明显肿大。患眼的角膜血管化且完全浑浊,角膜与巩膜之间没有清晰的边界。诊断为先天性青光眼,但由于解剖结构复杂和功能丧失,未进行手术。当孩子快3岁时,为防止角膜暴露引起并发症并改善外观,进行了眼球摘除术。

结果

对摘除眼球的形态学检查发现了文献中所称的“先天性前葡萄肿”或“先天性角膜葡萄肿”的典型表现,即巨大的葡萄肿样角膜伴浅表血管新生、Bowman层破坏、Descemet层及角膜内皮缺失。房角结构完全缺失,角膜后侧由色素上皮层覆盖,局部还有一层额外的无色素上皮内层。无前房。晶状体明显变小(小晶状体),部分嵌入角膜基质。睫状体的肌部和睫状部分离。细长、薄的睫状突向小晶状体延伸,而肌部完全被视网膜覆盖。

结论

这种罕见的复杂畸形综合征可轻易与原发性先天性青光眼区分开来,不应仅从概念上简化为角膜葡萄肿,因为这种葡萄肿只是整体的一部分。考虑到主要的形态学异常,我们更倾向于提出新术语“角膜葡萄肿 - 前房发育不全 - 小晶状体综合征(CSAMS)”。我们推测CSAMS可能是由于早期视杯前部的病理性融合所致。由于CSAMS患者的眼后段通常正常,葡萄肿切除联合巩膜角膜移植术可能是一种替代治疗选择,可避免眼球摘除并恢复可走动时的视力。

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