Wilson病合并圆锥角膜1例。

Adem Tellioglu, Derya Ozkan, Burcin Kepez Yildiz
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引用次数: 0

摘要

报告Wilson病(WD)合并圆锥角膜(KC) 1例。一位30岁男性,诊断为WD,因进行性双侧视力丧失而就诊于眼科。生物显微镜下发现双眼铜沉积环和轻度角膜中央扩张。病人有原发性震颤和轻度言语障碍。右眼角膜测量值K1 = 45.94屈光度(D), K2 = 49.10 D,左眼K1 = 47.14 D, K2 = 51.22 D。后侧仰角图上最大仰角点为右眼98 mm,左眼94 mm。双侧角膜地形图显示典型的KC型。基于这些发现,患者被诊断为KC,并建议角膜交联治疗。WD很少合并KC,仅有2例报告;这是迄今为止第三例WD合并KC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Wilson Disease Combined with Keratoconus: A Case Report.

Wilson Disease Combined with Keratoconus: A Case Report.

Wilson Disease Combined with Keratoconus: A Case Report.

Wilson Disease Combined with Keratoconus: A Case Report.

A case of Wilson disease (WD) combined with keratoconus (KC) is described. A 30-year-old male diagnosed with WD presented to Ophthalmology Department due to progressive bilateral vision loss. Biomicroscopy revealed copper depositional ring and mild central corneal ectasia in both eyes. The patient had essential tremors and mild speech disturbance. The keratometric values were K1 = 45.94 diopters (D), K2 = 49.10 D in the right eye, and K1 = 47.14 D, K2 = 51.22 D in the left eye. The maximal elevation points on the posterior elevation maps were 98 mm for the right eye and 94 mm for the left eye. The typical KC pattern was seen on corneal topography bilaterally. Based on these findings, the patient was diagnosed with KC, and corneal cross-linking treatment was recommended. WD rarely occurs in combination with KC, and only two cases have been reported; this is the third case of WD combined with KC so far.

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