Suppr超能文献

一例具有罕见角膜表现的非典型科根综合征病例。

A case of atypical Cogan's syndrome with uncommon corneal findings.

作者信息

Miserocchi E, Baltatzis S, Foster C S

机构信息

Ocular Immunology and Uveitis Service, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, USA.

出版信息

Cornea. 2001 Jul;20(5):540-2. doi: 10.1097/00003226-200107000-00021.

Abstract

PURPOSE

We report a case of atypical bilateral interstitial keratitis associated with Cogan's syndrome.

METHODS

A 28-year-old man presented with a 2-year history of recurrent bilateral keratitis. Bilateral hearing loss preceded the ocular symptoms by 2 years. The patient also complained of skin nodules, headache, back pain, and arthritis. Corneal finding were consistent with superior stromal keratitis with stromal neovascularization and lipid deposition in the stroma. The patient's audiogram revealed cochlear pathology compatible with Cogan's syndrome (sensorineural deafness).

RESULTS

The patient was treated with topical steroids but eventually required corneal transplantation in the right eye as a consequence of progressive loss of vision secondary to progressive lipid keratopathy. Visual acuity at the patient's most recent follow-up evaluation was 20/40.

CONCLUSION

This case represents an unusual type of interstitial keratitis associated with Cogan's disease. The absence of ocular symptoms at the time of initial ear involvement and the atypical presentation of the keratitis were responsible for the delay in diagnosis in this patient, resulting in hearing impairment.

摘要

目的

我们报告一例与科根综合征相关的非典型双侧间质性角膜炎病例。

方法

一名28岁男性,有2年复发性双侧角膜炎病史。双侧听力丧失比眼部症状早2年出现。患者还主诉有皮肤结节、头痛、背痛和关节炎。角膜检查结果符合上皮下基质角膜炎,伴有基质新生血管形成和基质脂质沉积。患者的听力图显示耳蜗病变符合科根综合征(感音神经性耳聋)。

结果

患者接受了局部类固醇治疗,但最终因进行性脂质角膜病变导致视力逐渐丧失,右眼需要进行角膜移植。患者最近一次随访评估时的视力为20/40。

结论

该病例代表了一种与科根病相关的不寻常类型的间质性角膜炎。最初耳部受累时无眼部症状以及角膜炎的非典型表现导致了该患者诊断延迟,进而导致听力损害。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验