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彼得斯异常合并突出性角膜假葡萄肿。

Peters' anomaly associated with protruding corneal pseudo staphyloma.

作者信息

Zaidman G W, Juechter K

机构信息

Westchester Medical Center, Our Lady of Mercy Hospital, New York Medical College, Department of Ophthalmology, Valhalla 10595, USA.

出版信息

Cornea. 1998 Mar;17(2):163-8. doi: 10.1097/00003226-199803000-00008.

Abstract

PURPOSE

To describe a new manifestation of Peters' anomaly.

METHODS

We managed four infants with an unusual form of Peters' anomaly. One eye of each patient had a thickened and scarred cornea, mimicking a corneal staphyloma, protruding anteriorly from the corneal plane. The other eye of each patient ranged from normal to having severe ocular anomalies. A corneal transplant was performed in each case.

RESULTS

Follow-up ranged from 1 to 3 years. Three eyes maintained graft clarity for at least 1 year. Each of these eyes developed vision. Two of these eyes developed glaucoma. The one eye with graft failure developed an inoperable retinal detachment. The histopathology of each corneal button showed changes consistent with Peters' anomaly.

CONCLUSIONS

These corneas demonstrated characteristics of both Peters' anomaly and congenital anterior staphyloma. Despite their severe anomalies, surgery successfully restored a more normal cosmetic appearance in all four eyes and vision in three eyes.

摘要

目的

描述彼得斯异常的一种新表现形式。

方法

我们诊治了4例具有不寻常形式彼得斯异常的婴儿。每位患者的一只眼睛角膜增厚且有瘢痕,类似角膜葡萄肿,从角膜平面向前突出。每位患者的另一只眼睛情况从正常到有严重眼部异常不等。每例均进行了角膜移植。

结果

随访时间为1至3年。三只眼睛的移植片至少保持了1年的透明。这些眼睛均获得了视力。其中两只眼睛发生了青光眼。移植失败的那只眼睛出现了无法手术治疗的视网膜脱离。每个角膜植片的组织病理学表现均与彼得斯异常相符。

结论

这些角膜表现出彼得斯异常和先天性前葡萄肿的特征。尽管存在严重异常,但手术成功使所有四只眼睛的外观更接近正常,三只眼睛恢复了视力。

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