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与后部多形性角膜营养不良相关的厚圆锥角膜

Thick keratoconic cornea associated with posterior polymorphous corneal dystrophy.

作者信息

Zaarour K, Slim E, Antoun J, Waked N

机构信息

Ophthalmology department, Hôtel-Dieu de France, Saint-Joseph University (USJ), faculty of medicine, Alfred Naccache Street, Achrafieh, Beirut, Lebanon.

Ophthalmology department, Hôtel-Dieu de France, Saint-Joseph University (USJ), faculty of medicine, Alfred Naccache Street, Achrafieh, Beirut, Lebanon.

出版信息

J Fr Ophtalmol. 2017 Mar;40(3):232-236. doi: 10.1016/j.jfo.2016.09.014. Epub 2017 Jan 13.

Abstract

INTRODUCTION

We herein report a case of bilateral unusually thick non-edematous keratoconic corneas with associated endothelial features of posterior polymorphous corneal dystrophy (PPCD).

CASE REPORT

We report the case of a 27-year-old myopic woman who presented for refractive surgery. Slit lamp exam showed bilateral corneal protrusion with diffuse deep stromal and endothelial vesicular opacities and small paracentral bands. Topography showed generalized advanced corneal steepening in both eyes with increased anterior and posterior central corneal elevations in comparison to the best fit sphere. Ultrasound pachymetry showed central corneal thickness of 605μm (RE) and 612μm (LE). On specular biomicroscopy, cell density of 2503 cells/mm RE and 1526 cells/mm LE with significant cellular pleomorphism and polymegathism were noted.

DISCUSSION

Clinical and paraclinical findings together suggest the presence of simultaneous keratoconus and PPCD. The literature has suggested an association between PPCD and steep cornea. Moreover, many reports have also described cases of associated PPCD and keratoconus with characteristic thinning and ectasia, in comparison to the unusual thick corneas noted in our patient, despite the absence of edema. Identification of genetics factors is further needed to clarify this association.

CONCLUSION

This case describes a patient whose corneas present features of both keratoconus and PPCD and is unique due to the presence of increased corneal thickness despite the absence of edema.

摘要

引言

我们在此报告一例双侧角膜异常增厚且无水肿的圆锥角膜病例,伴有后多形性角膜营养不良(PPCD)的内皮特征。

病例报告

我们报告一名27岁近视女性的病例,该患者前来接受屈光手术。裂隙灯检查显示双侧角膜突出,伴有弥漫性深层基质和内皮水泡样混浊以及小的旁中央带。角膜地形图显示双眼均有广泛性晚期角膜陡峭,与最佳拟合球面相比,中央角膜前后表面高度增加。超声角膜测厚显示右眼中央角膜厚度为605μm,左眼为612μm。在镜面显微镜检查中,右眼细胞密度为2503个细胞/mm,左眼为1526个细胞/mm,可见明显的细胞多形性和大小不均。

讨论

临床和辅助检查结果共同提示同时存在圆锥角膜和PPCD。文献表明PPCD与陡峭角膜之间存在关联。此外,许多报告也描述了PPCD与圆锥角膜相关的病例,其具有特征性的变薄和扩张,与我们患者中观察到的异常增厚角膜不同,尽管没有水肿。进一步需要确定遗传因素以阐明这种关联。

结论

本病例描述了一名角膜呈现圆锥角膜和PPCD特征的患者,因其角膜厚度增加且无水肿而具有独特性。

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