• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

[一例伴有广泛视网膜脉络膜萎缩的后巩膜炎]

[A case of posterior scleritis associated with extensive retinochoroidal atrophy].

作者信息

Minami Rieko, Saito Wataru, Namba Kenichi, Ohno Shigeaki

机构信息

Department of Ophthalmology and Visual Sciences, Hokkaido University Graduate School of Medicine, N 15, W 7, Kita-ku, Sapporo 060-8638, Japan.

出版信息

Nippon Ganka Gakkai Zasshi. 2006 Sep;110(9):730-5.

PMID:17025231
Abstract

BACKGROUND

Posterior scleritis is known to exhibit various changes in the ocular fundus, but retinochoroidal atrophy is a rare complication.

CASE

A 54-year-old man presented with the complaint of blurred vision in the right eye. The patient had visited our clinic twice before, 22 and 11 years earlier. Although his funduscopic findings had demonstrated choroidal detachment in both eyes, the cause could not be determined at that time.

FINDINGS

His visual acuity was 20/200, OD and 20/100, OS. Funduscopic examination showed annual choroidal detachments and geographic retinochoroidal atrophy in the posterior pole OU, and serous retinal detachment OD. B-scan ultrasonograpy revealed diffuse thickening and flattening of the posterior coats of the eye, and orbital enhanced computed tomography revealed thickening and enhancement of the posterior sclera. A diagnosis of posterior scleritis was made. Prednisolone 80 mg/ day was initiated and gradually tapered. Nine months later choroidal and serous retinal detachment were resolved.

CONCLUSION

We encountered a rare case of posterior scleritis with associated extensive retinochoroidal atrophy. We speculated that the cause was inflammation of the retina and choroid, and accumulation of subretinal fluid for a long period.

摘要

背景

已知后巩膜炎可导致眼底出现各种变化,但视网膜脉络膜萎缩是一种罕见的并发症。

病例

一名54岁男性因右眼视力模糊前来就诊。该患者在22年前和11年前曾两次到我们诊所就诊。尽管当时眼底检查发现双眼脉络膜脱离,但病因未明确。

检查结果

其右眼视力为20/200,左眼视力为20/100。眼底检查显示双眼后极部有每年发作的脉络膜脱离和地图状视网膜脉络膜萎缩,右眼有浆液性视网膜脱离。B超检查显示眼球后部脉络膜弥漫性增厚和平坦,眼眶增强计算机断层扫描显示后巩膜增厚和强化。诊断为后巩膜炎。开始使用泼尼松龙80毫克/天,并逐渐减量。九个月后,脉络膜和浆液性视网膜脱离消失。

结论

我们遇到了一例罕见的伴有广泛视网膜脉络膜萎缩的后巩膜炎病例。我们推测病因是视网膜和脉络膜炎症以及长期视网膜下液积聚。

相似文献

1
[A case of posterior scleritis associated with extensive retinochoroidal atrophy].[一例伴有广泛视网膜脉络膜萎缩的后巩膜炎]
Nippon Ganka Gakkai Zasshi. 2006 Sep;110(9):730-5.
2
Alterations in choroidal circulatory dynamics and choroidal thickness before and after treatment in posterior scleritis.后部巩膜炎治疗前后脉络膜循环动力学和脉络膜厚度的变化。
BMC Ophthalmol. 2023 Sep 19;23(1):382. doi: 10.1186/s12886-023-03140-8.
3
A Case of Refractory Posterior Scleritis with Marked Retinochoroidal Detachment Associated with Panuveitis.一例伴有全葡萄膜炎的难治性后部巩膜炎伴明显视网膜脉络膜脱离。
Tokai J Exp Clin Med. 2024 Jul 20;49(2):85-88.
4
Posterior scleritis with secondary ciliochoroidal effusion.后巩膜炎伴继发性睫状体脉络膜积液。
J Am Optom Assoc. 1989 Apr;60(4):300-6.
5
Optical coherence tomography findings in a child with posterior scleritis.一名患有后巩膜炎儿童的光学相干断层扫描结果
Eur J Ophthalmol. 2008 Nov-Dec;18(6):1007-10. doi: 10.1177/112067210801800625.
6
Choroidal observations in posterior scleritis using high-penetration optical coherence tomography.使用高穿透性光学相干断层扫描技术对后巩膜炎的脉络膜观察
Int Ophthalmol. 2014 Aug;34(4):937-43. doi: 10.1007/s10792-013-9894-4. Epub 2014 Jan 8.
7
Posterior Scleritis.后巩膜炎
Ophthalmic Surg Lasers Imaging Retina. 2019 Oct 1;50(10):660. doi: 10.3928/23258160-20191009-11.
8
[Pigmented paravenous retinochoroidal atrophy--a case report].[色素性静脉旁视网膜脉络膜萎缩——病例报告]
Klin Oczna. 2014;116(2):115-8.
9
Giant nodular posterior scleritis simulating choroidal melanoma.模拟脉络膜黑色素瘤的巨大结节性后巩膜炎。
Indian J Ophthalmol. 2006 Jun;54(2):120-2. doi: 10.4103/0301-4738.25835.
10
Posterior scleritis presenting as conjunctivitis in a child.一名儿童后巩膜炎表现为结膜炎。
BMJ Case Rep. 2016 Dec 9;2016:bcr2016217968. doi: 10.1136/bcr-2016-217968.