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下矛状晶状体混浊作为圆锥角膜的体征

Inferior Spear-like Lens Opacity as a Sign of Keratoconus.

作者信息

Salouti Ramin, Khosravi Amir, Fardaei Majid, Zamani Mohammad, Nejabat Mahmoud, Ghoreyshi Maryam, Yazdanpanah Mahboobeh, Salouti Kia, Nowroozzadeh M Hossein

机构信息

Department of Ophthalmology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Salouti Cornea Research Center, Salouti Eye Clinic, Shiraz, Iran.

出版信息

J Ophthalmic Vis Res. 2022 Jan 21;17(1):12-18. doi: 10.18502/jovr.v17i1.10165. eCollection 2022 Jan-Mar.

Abstract

PURPOSE

To report 21 cases of typical inferior feather-shape lens opacity associated with keratoconus.

METHODS

In this cross-sectional study, we evaluated the association of keratoconus with inferior feather-shape lens opacity in refractive surgery candidates. Visual acuity, demographic, refractive, and topographic characteristics of 26 eyes of 21 patients with inferior feather-shape lens opacity were evaluated in detail. Pedigree analysis was also performed to assess possible inheritance.

RESULTS

Overall, 2122 out of 33,368 cases (6.4%) without lens opacity had keratoconus, while 20 out of 21 patients (95.2%) with peculiar lens opacity had definite keratoconus ( 0.001). Lens opacity was bilateral in 5 cases (24%), and keratoconus was bilateral in all 20 patients with lens opacity. Nine eyes out of thirty-six with a complete data record (25%) had a severe keratoconus and underwent deep lamellar keratoplasty, while 11 (31%) had forme fruste keratoconus. Pedigrees were drawn for eight patients, most families of whom suggested an X-linked recessive inheritance.

CONCLUSION

The present study was the first to investigate patients with a peculiar inferior feather-shape lens opacity accompanied by bilateral keratoconus, which was observed in 95% of the patients. This finding should raise awareness as to the possibility of diagnosing keratoconus in the eyes of the patients with these characteristics.

摘要

目的

报告21例与圆锥角膜相关的典型下羽毛状晶状体混浊病例。

方法

在这项横断面研究中,我们评估了圆锥角膜与屈光手术候选者中下羽毛状晶状体混浊之间的关联。详细评估了21例患有下羽毛状晶状体混浊患者的26只眼的视力、人口统计学、屈光和地形特征。还进行了系谱分析以评估可能的遗传情况。

结果

总体而言,33368例无晶状体混浊的病例中有2122例(6.4%)患有圆锥角膜,而21例患有特殊晶状体混浊的患者中有20例(95.2%)患有明确的圆锥角膜(P<0.001)。晶状体混浊为双侧的有5例(24%),所有20例有晶状体混浊的患者圆锥角膜均为双侧。36只眼中有9只(25%)有完整数据记录,患有严重圆锥角膜并接受了深层板层角膜移植术,11只眼(31%)患有顿挫型圆锥角膜。为8例患者绘制了系谱,其中大多数家族提示X连锁隐性遗传。

结论

本研究首次对伴有双侧圆锥角膜的特殊下羽毛状晶状体混浊患者进行了调查,95%的患者出现这种情况。这一发现应提高人们对具有这些特征的患者眼中圆锥角膜诊断可能性的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/549d/8850847/1e68f24d240b/jovr-17-12-g001.jpg

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