Suppr超能文献

韦尔-马钱综合征合并青光眼晚期及角膜内皮功能障碍:病例报告及文献复习。

Weill-Marchesani syndrome with advanced glaucoma and corneal endothelial dysfunction: a case report and literature review.

机构信息

Department of Ophthalmology, Qilu Hospital of Shandong University, Jinan, China.

出版信息

BMC Ophthalmol. 2015 Jan 9;15:3. doi: 10.1186/1471-2415-15-3.

Abstract

BACKGROUND

To report the diagnostic features and management strategy of a rare case of Weill-Marchesani syndrome with advanced glaucoma and corneal endothelial dysfunction.

CASE PRESENTATION

A patient presented with advanced glaucoma with an intraocular pressure of 49 mmHg in the left eye, and subsequently received trabeculectomy to control the intraocular pressure. Surprisingly, slit lamp examination through the dilated pupil revealed a dislocated microspherophakic lens almost touching the corneal endothelium. A microspherophakic lens was confirmed by anterior segment optical coherence tomography. Weill-Marchesani syndrome was then diagnosed by ocular examinations, and was accompanied by systemic abnormalities, including brachymorphia and brachydactyly. Corneal endothelial microscopy showed severe corneal endothelial dysfunction, and lens extraction and intraocular lens implantation were subsequently performed to prevent further endothelial damage. At the 1-year follow-up visit, the patient had well-controlled intraocular pressure, transparent cornea, and normal anterior chamber depth, while the intraocular lens remained correctly in place.

CONCLUSIONS

Weill-Marchesani syndrome could be diagnosed by microspherophakia, high myopia, secondary glaucoma, and systemic abnormalities such as brachymorphia and brachydactyly. Removal of the microspherophakia is recommended to control intraocular pressure and improve vision. Advanced glaucoma in Weill-Marchesani syndrome should be treated with combined glaucoma surgery and lens extraction.

摘要

背景

报告一例罕见的 Weill-Marchesani 综合征伴晚期青光眼和角膜内皮功能障碍的诊断特征和治疗策略。

病例介绍

患者左眼眼压高达 49mmHg,表现为晚期青光眼,随后接受小梁切除术以控制眼压。令人惊讶的是,通过扩瞳后的裂隙灯检查发现一个晶状体脱位的微小球形晶状体,几乎触及角膜内皮。前节光学相干断层扫描证实为微小球形晶状体。通过眼部检查诊断为 Weill-Marchesani 综合征,同时伴有全身性异常,包括短肢畸形和短指畸形。角膜内皮显微镜显示严重的角膜内皮功能障碍,随后进行晶状体摘除和人工晶状体植入术,以防止进一步的内皮损伤。在 1 年的随访中,患者眼压得到良好控制,角膜透明,前房深度正常,人工晶状体位置正常。

结论

Weill-Marchesani 综合征可通过小眼球、高度近视、继发性青光眼以及短肢畸形和短指畸形等全身异常来诊断。建议摘除微小球形晶状体以控制眼压并提高视力。Weill-Marchesani 综合征的晚期青光眼应采用联合青光眼手术和晶状体摘除进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ebb/4298062/039e40eb3838/12886_2014_528_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验