• 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

Vogt-小柳-原田病的后节复发

Posterior segment recurrences in Vogt-Koyanagi-Harada disease.

作者信息

Sachdev Nishant, Gupta Vishali, Gupta Amod, Singh Ramandeep

机构信息

Department of Ophthalmology, Post Graduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India.

出版信息

Int Ophthalmol. 2008 Oct;28(5):339-45. doi: 10.1007/s10792-007-9144-8. Epub 2007 Sep 26.

DOI:10.1007/s10792-007-9144-8
PMID:17898934
Abstract

AIM

To describe the clinical profile, management, and outcome in seven patients with posterior segment recurrence in Vogt-Koyanagi-Harada (VKH) disease.

MATERIAL AND METHODS

Retrospective chart review of all the patients of VKH disease presenting to our institute between 2001 and 2005 was carried out. Patients with a documented posterior segment recurrence during follow-up were included in this study. Their history, systemic associations, ocular findings, investigations, management strategies, and treatment response were noted.

RESULTS

Out of 82 VKH patients screened, documented posterior segment recurrence was seen in seven patients who included five women and two men, with a mean age of 33.7 years (range 22-55 years). At onset, two patients had incomplete and five had probable VKH disease. At the time of recurrence, four patients were on maintenance dose (5-10 mg/day) of oral corticosteroid while the remaining three were off treatment. The mean interval between the primary episode and posterior segment recurrence was 33.7 weeks (range 16-52 weeks). All posterior segment recurrences were bilateral and were characterized by vitritis (eight eyes), papillitis (14 eyes), multiple yellow-white oval subretinal lesions (six eyes), and exudative retinal detachment (10 eyes). The recurrences were managed with oral corticosteroids (1.0-1.5 mg/day) and Azathioprine (2.0-2.5 mg/day). Subsequently, three patients experienced a second episode of posterior segment recurrence, which also responded to the corticosteroid-Azathioprine combination.

CONCLUSIONS

Recurrences in VKH disease may involve predominantly the posterior segment, and respond well to the standard treatment.

摘要

目的

描述7例Vogt-小柳-原田(VKH)病后段复发患者的临床特征、治疗及预后。

材料与方法

对2001年至2005年间在我院就诊的所有VKH病患者进行回顾性病历审查。纳入随访期间有后段复发记录的患者。记录他们的病史、全身关联情况、眼部检查结果、检查、治疗策略及治疗反应。

结果

在筛查的82例VKH患者中,7例有后段复发记录,其中5例女性,2例男性,平均年龄33.7岁(范围22 - 55岁)。发病时,2例患者为不完全型,5例可能为VKH病。复发时,4例患者正在口服糖皮质激素维持剂量(5 - 10毫克/天),其余3例已停止治疗。初次发作与后段复发的平均间隔时间为33.7周(范围16 - 52周)。所有后段复发均为双侧,表现为玻璃体炎(8只眼)、视乳头炎(14只眼)、多个黄白色椭圆形视网膜下病变(6只眼)和渗出性视网膜脱离(10只眼)。复发采用口服糖皮质激素(1.0 - 1.5毫克/天)和硫唑嘌呤(2.0 - 2.5毫克/天)治疗。随后,3例患者经历了第二次后段复发,对糖皮质激素 - 硫唑嘌呤联合治疗也有反应。

结论

VKH病的复发可能主要累及后段,对标准治疗反应良好。

相似文献

1
Posterior segment recurrences in Vogt-Koyanagi-Harada disease.Vogt-小柳-原田病的后节复发
Int Ophthalmol. 2008 Oct;28(5):339-45. doi: 10.1007/s10792-007-9144-8. Epub 2007 Sep 26.
2
The outcomes of mycophenolate mofetil therapy combined with systemic corticosteroids in acute uveitis associated with Vogt-Koyanagi-Harada disease.霉酚酸酯联合全身皮质类固醇治疗伴 Vogt-小柳原田病的急性葡萄膜炎的疗效。
Acta Ophthalmol. 2012 Dec;90(8):e603-8. doi: 10.1111/j.1755-3768.2012.02498.x. Epub 2012 Sep 12.
3
Clinical features and visual outcomes of 111 patients with new-onset acute Vogt-Koyanagi-Harada disease treated with pulse intravenous corticosteroids.111 例新发急性 Vogt-小柳原田病患者采用脉冲静脉内皮质类固醇治疗的临床特征和视力结果。
Br J Ophthalmol. 2019 Feb;103(2):274-278. doi: 10.1136/bjophthalmol-2017-311691. Epub 2018 Apr 17.
4
Prognostic factors for clinical outcomes in patients with Vogt-Koyanagi-Harada disease treated with high-dose corticosteroids.大剂量皮质类固醇治疗 Vogt-Koyanagi-Harada 病患者的临床转归的预后因素。
Acta Ophthalmol. 2013 Sep;91(6):e486-93. doi: 10.1111/aos.12127. Epub 2013 Apr 10.
5
Incidence and clinical features of recurrent Vogt-Koyanagi-Harada disease in Japanese individuals.日本人群中复发性Vogt-小柳-原田病的发病率及临床特征
Jpn J Ophthalmol. 2015 May;59(3):157-63. doi: 10.1007/s10384-015-0377-1. Epub 2015 Mar 26.
6
Clinical Outcomes of Patients with Vogt-Koyanagi-Harada Disease Over 12 Years at a Tertiary Center.一家三级医疗中心12年间Vogt-小柳-原田病患者的临床结局
Ocul Immunol Inflamm. 2016 Oct;24(5):521-9. doi: 10.3109/09273948.2015.1025984. Epub 2015 Sep 23.
7
A case of probable Vogt-Koyanagi-Harada disease in a 3-year-old girl.一例三岁女童疑诊 Vogt-Koyanagi-Harada 病。
BMC Ophthalmol. 2019 Aug 13;19(1):179. doi: 10.1186/s12886-019-1192-0.
8
Acute phase clinical manifestations of patients with Vogt-Koyanagi-Harada disease in Southern China.中国南方 Vogt-Koyanagi-Harada 病患者的急性期临床表现。
BMC Ophthalmol. 2023 May 5;23(1):199. doi: 10.1186/s12886-023-02952-y.
9
Mycophenolate mofetil combined with systemic corticosteroids prevents progression to chronic recurrent inflammation and development of 'sunset glow fundus' in initial-onset acute uveitis associated with Vogt-Koyanagi-Harada disease.霉酚酸酯联合全身用糖皮质激素可预防与Vogt-小柳-原田病相关的初发性急性葡萄膜炎进展为慢性复发性炎症和“晚霞眼底”的形成。
Acta Ophthalmol. 2017 Feb;95(1):85-90. doi: 10.1111/aos.13189. Epub 2016 Aug 18.
10
Vogt-Koyanagi-Harada disease presenting as acute angle closure glaucoma at onset.Vogt-Koyanagi-Harada 病发病时表现为急性闭角型青光眼。
Clin Exp Ophthalmol. 2011 Sep-Oct;39(7):639-47. doi: 10.1111/j.1442-9071.2011.02523.x. Epub 2011 Apr 4.

引用本文的文献

1
Vogt-Koyanagi-Harada Disease and COVID.伏格特-小柳-原田病与新冠病毒
J Clin Med. 2023 Sep 27;12(19):6242. doi: 10.3390/jcm12196242.
2
Immunosuppressive therapy for Vogt-Koyanagi-Harada disease: a retrospective study and review of literature.伏格特-小柳-原田病的免疫抑制治疗:一项回顾性研究及文献综述
J Ophthalmic Inflamm Infect. 2023 May 19;13(1):27. doi: 10.1186/s12348-023-00333-6.
3
Incidence and clinical features of recurrent Vogt-Koyanagi-Harada disease in Japanese individuals.日本人群中复发性Vogt-小柳-原田病的发病率及临床特征

本文引用的文献

1
Indocyanine green angiography in Vogt-Koyanagi-Harada disease: angiographic signs and utility in patient follow-up.吲哚菁绿血管造影在Vogt-小柳-原田病中的应用:血管造影征象及在患者随访中的作用
Int Ophthalmol. 2007 Apr-Jun;27(2-3):173-82. doi: 10.1007/s10792-007-9060-y. Epub 2007 Apr 25.
2
Peripheral iris depigmentation and ocular hypotony: result of the natural course of non-treated Vogt-Koyanagi-Harada (VKH) disease.周边虹膜色素脱失与低眼压:未治疗的小柳原田病(VKH)自然病程的结果
Int Ophthalmol. 2007 Apr-Jun;27(2-3):221-2. doi: 10.1007/s10792-007-9048-7. Epub 2007 Feb 23.
3
Recurrent anterior uveitis in patients with Vogt-Koyanagi-Harada syndrome.
Jpn J Ophthalmol. 2015 May;59(3):157-63. doi: 10.1007/s10384-015-0377-1. Epub 2015 Mar 26.
伏格特-小柳-原田综合征患者的复发性前葡萄膜炎。
Arch Ophthalmol. 2004 Jun;122(6):922-3. doi: 10.1001/archopht.122.6.922.
4
UVEOMENINGOENCEPHALITIC SYNDROME (VOGT-KOYANAGI-HARADA).葡萄膜脑膜脑炎综合征(伏格特-小柳-原田综合征)
Arch Neurol. 1965 Feb;12:197-205. doi: 10.1001/archneur.1965.00460260087010.
5
Frosted branch angiitis associated with Harada disease-like manifestations recurs 10 years later.伴有原田病样表现的霜样树枝状视网膜血管炎10年后复发。
Jpn J Ophthalmol. 2002 Nov-Dec;46(6):682-4. doi: 10.1016/s0021-5155(02)00564-6.
6
Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature.Vogt-小柳-原田病修订诊断标准:国际命名委员会报告
Am J Ophthalmol. 2001 May;131(5):647-52. doi: 10.1016/s0002-9394(01)00925-4.
7
The contribution of indocyanine green angiography to the appraisal and management of Vogt-Koyanagi-Harada disease.吲哚青绿血管造影在Vogt-小柳-原田病评估与治疗中的作用。
Ophthalmology. 2001 Jan;108(1):54-64. doi: 10.1016/s0161-6420(00)00428-0.
8
Multiple recurrences of exudative retinal detachment in a patient with Vogt-Koyanagi-Harada disease.Vogt-小柳-原田病患者出现多次渗出性视网膜脱离复发。
Retina. 2000;20(6):672-4. doi: 10.1097/00006982-200006000-00017.
9
Tyrosinase family proteins are antigens specific to Vogt-Koyanagi-Harada disease.酪氨酸酶家族蛋白是小柳原田病特有的抗原。
J Immunol. 2000 Dec 15;165(12):7323-9. doi: 10.4049/jimmunol.165.12.7323.
10
Vogt-Koyanagi-Harada syndrome.伏格特-小柳-原田综合征
Surv Ophthalmol. 1995 Jan-Feb;39(4):265-92. doi: 10.1016/s0039-6257(05)80105-5.