• 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

一名44岁I型面肩肱型肌营养不良患者的似科茨病的管理

Management of Coats-Like Disease in a Forty-Four-Year-Old Patient with FSHD Type I.

作者信息

Bruzzone Francesca, Beltraminelli Tim, Casanova Alex, Menghini Moreno

机构信息

Clinica di Oftalmologia, Ospedale Regionale di Lugano, Ente Ospedaliero Cantonale (EOC), Lugano, Switzerland.

出版信息

Case Rep Ophthalmol. 2023 Jun 16;14(1):250-256. doi: 10.1159/000531007. eCollection 2023 Jan-Dec.

DOI:10.1159/000531007
PMID:37383166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10294264/
Abstract

A forty-four-year-old female patient known for FSHD type I, with unremarkable past ocular history, complained of progressive visual acuity deterioration during a routine ophthalmological visit. Best-corrected visual acuity (BCVA) was 1.0 decimal Snellen equivalent bilaterally. Dilated fundus examination showed evidence of retinal Coats-like disease in the left eye, while the right eye showed significant retinal vascular tortuosity. Multimodal examinations (OCT scans and FA-fluorescein angiography) revealed large areas of retinal ischemia, thus confirming a retinal vascular disorder compatible with the diagnosis of Coats-like disease. Left eye laser photocoagulation of the ischemic areas was performed to avoid neovascular complications that had not been detected during follow-up visits (12 months), and BCVA in the left eye remained stable at 1.0 decimals Snellen equivalent. Coats-like disease in a patient affected by FSHD type I should always be screened even in the absence of any prior ocular diseases. Guidelines concerning the ophthalmological management of adults affected by FSHD are lacking. Based on this case, we recommend performing a yearly complete ophthalmological checkup with dilated fundus examination and retinal imaging. Patients should, furthermore, be encouraged to seek medical attention when noticing deterioration of visual acuity or other visual symptoms in order to avoid missing potential sight-threatening ocular complications.

摘要

一名44岁的I型面肩肱型肌营养不良(FSHD)女性患者,既往眼部病史无异常,在一次常规眼科检查中抱怨视力逐渐下降。双眼最佳矫正视力(BCVA)均为小数记法的1.0(相当于Snellen视力表的20/20)。散瞳眼底检查显示左眼有视网膜Coats样病迹象,而右眼则有明显的视网膜血管迂曲。多模式检查(光学相干断层扫描[OCT]和荧光素血管造影[FA])显示视网膜大面积缺血,从而证实存在与Coats样病诊断相符的视网膜血管疾病。对左眼缺血区域进行了激光光凝治疗,以避免在随访(12个月)期间未检测到的新生血管并发症,左眼的BCVA保持稳定,为小数记法的1.0(相当于Snellen视力表的20/20)。即使在没有任何既往眼部疾病的情况下,也应始终对I型FSHD患者进行Coats样病筛查。目前缺乏关于FSHD成年患者眼科管理的指南。基于此病例,我们建议每年进行一次全面的眼科检查,包括散瞳眼底检查和视网膜成像。此外,应鼓励患者在发现视力下降或其他视觉症状时寻求医疗关注,以避免错过潜在的威胁视力的眼部并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/ba018b3bb42e/cop-2023-0014-0001-531007_F03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/fbd2d33ba8bf/cop-2023-0014-0001-531007_F01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/beb410acdec6/cop-2023-0014-0001-531007_F02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/ba018b3bb42e/cop-2023-0014-0001-531007_F03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/fbd2d33ba8bf/cop-2023-0014-0001-531007_F01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/beb410acdec6/cop-2023-0014-0001-531007_F02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094b/10294264/ba018b3bb42e/cop-2023-0014-0001-531007_F03.jpg

相似文献

1
Management of Coats-Like Disease in a Forty-Four-Year-Old Patient with FSHD Type I.一名44岁I型面肩肱型肌营养不良患者的似科茨病的管理
Case Rep Ophthalmol. 2023 Jun 16;14(1):250-256. doi: 10.1159/000531007. eCollection 2023 Jan-Dec.
2
Combined treatment with intravitreal bevacizumab and laser photocoagulation for exudative maculopathy in facioscapulohumeral muscular dystrophy.玻璃体内注射贝伐单抗联合激光光凝治疗面肩肱型肌营养不良症的渗出性黄斑病变。
Ophthalmic Genet. 2017 Sep-Oct;38(5):490-493. doi: 10.1080/13816810.2017.1279183. Epub 2017 Jan 25.
3
Coats-like retinopathy in an infant with preclinical facioscapulohumeral dystrophy.患有临床前期面肩肱型肌营养不良的婴儿的类科茨病性视网膜病变。
J AAPOS. 2012 Apr;16(2):204-6. doi: 10.1016/j.jaapos.2011.11.005.
4
Reemergence of dormant Coats disease after 30 years.30年后静止期寇茨病再度出现。
Eur J Ophthalmol. 2012 May-Jun;22(3):509-12. doi: 10.5301/ejo.5000040.
5
Multimodal Imaging Findings in Retinopathy Associated with Facioscapulohumeral Muscular Dystrophy before and after Treatment with Intravitreal Aflibercept and Laser Photocoagulation.玻璃体内注射阿柏西普和激光光凝治疗前后面肩肱型肌营养不良相关视网膜病变的多模态影像学表现
Case Rep Ophthalmol. 2022 Jul 14;13(2):556-561. doi: 10.1159/000525797. eCollection 2022 May-Aug.
6
TWO-YEAR RESULTS OF INTRAVITREAL INJECTIONS OF AFLIBERCEPT IN COATS DISEASE: A CASE REPORT.眼 coats 病患者玻璃体内注射 aflibercept 的两年疗效:病例报告。
Retin Cases Brief Rep. 2022 Jul 1;16(4):473-478. doi: 10.1097/ICB.0000000000001011.
7
Diagnosis and clinical course of ocular ischemic syndrome with retinal vascular abnormalities due to unilateral ocular artery and internal carotid artery stenosis in a child with neurofibromatosis type 1: a case report.诊断和临床表现为单侧眼动脉和颈内动脉狭窄导致的儿童 1 型神经纤维瘤病视网膜血管异常的眼缺血综合征:病例报告。
BMC Ophthalmol. 2020 Oct 23;20(1):426. doi: 10.1186/s12886-020-01670-z.
8
Intravitreal bevacizumab injections combined with laser photocoagulation for adult-onset Coats' disease.玻璃体内注射贝伐单抗联合激光光凝治疗成人期Coats病
Graefes Arch Clin Exp Ophthalmol. 2016 Aug;254(8):1511-1517. doi: 10.1007/s00417-015-3233-6. Epub 2015 Dec 3.
9
Three-year follow-up of Coats disease treated with conbercept and 532-nm laser photocoagulation.康柏西普联合532纳米激光光凝治疗Coats病的三年随访
World J Clin Cases. 2020 Dec 26;8(24):6243-6251. doi: 10.12998/wjcc.v8.i24.6243.
10
Fluorescein Angiographic Abnormalities in the Contralateral Eye with Normal Fundus in Children with Unilateral Coats' Disease.单侧科茨病患儿对侧眼底正常眼中的荧光素血管造影异常
Korean J Ophthalmol. 2018 Feb;32(1):65-69. doi: 10.3341/kjo.2016.0092. Epub 2018 Jan 25.

本文引用的文献

1
Phenotype of Coats disease in females.女性型 Coats 病的表型。
BMJ Open Ophthalmol. 2022 Feb 4;7(1):e000883. doi: 10.1136/bmjophth-2021-000883. eCollection 2022.
2
Ophthalmological findings in facioscapulohumeral dystrophy.面肩肱型肌营养不良症的眼科表现
Brain Commun. 2019 Oct 11;1(1):fcz023. doi: 10.1093/braincomms/fcz023. eCollection 2019.
3
Coats disease: An overview of classification, management and outcomes. coats 病:分类、管理和结果概述。
Indian J Ophthalmol. 2019 Jun;67(6):763-771. doi: 10.4103/ijo.IJO_841_19.
4
Facioscapulohumeral Muscular Dystrophy: Update on Pathogenesis and Future Treatments.面肩肱型肌营养不良症:发病机制和未来治疗方法的最新进展。
Neurotherapeutics. 2018 Oct;15(4):863-871. doi: 10.1007/s13311-018-00675-3.
5
Facioscapulohumeral Muscular Dystrophy.面肩肱型肌营养不良症
Continuum (Minneap Minn). 2016 Dec;22(6, Muscle and Neuromuscular Junction Disorders):1916-1931. doi: 10.1212/CON.0000000000000399.
6
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy.DNMT3B基因的突变会改变D4Z4重复序列的表观遗传抑制作用以及面肩肱型肌营养不良症的外显率。
Am J Hum Genet. 2016 May 5;98(5):1020-1029. doi: 10.1016/j.ajhg.2016.03.013.
7
Coats syndrome in facioscapulohumeral dystrophy type 1: frequency and D4Z4 contraction size.1 型面肩肱型肌营养不良症中的 Coats 综合征:频率和 D4Z4 收缩大小。
Neurology. 2013 Mar 26;80(13):1247-50. doi: 10.1212/WNL.0b013e3182897116. Epub 2013 Feb 27.
8
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.SMCHD1 突变与 FSHD 许可的 D4Z4 等位基因的双基因遗传导致 2 型面肩肱型肌营养不良症。
Nat Genet. 2012 Dec;44(12):1370-4. doi: 10.1038/ng.2454. Epub 2012 Nov 11.
9
Subclinical facioscapulohumeral muscular dystrophy masquerading as bilateral Coats disease in a woman.一名女性患者中,亚临床型面肩肱型肌营养不良症伪装成双侧科茨病。
Arch Ophthalmol. 2011 Jun;129(6):807-9. doi: 10.1001/archophthalmol.2011.124.
10
A population-based study of Coats disease in the United Kingdom I: epidemiology and clinical features at diagnosis.基于人群的英国 Coats 病研究 I:诊断时的流行病学和临床特征。
Eye (Lond). 2010 Dec;24(12):1797-801. doi: 10.1038/eye.2010.126. Epub 2010 Sep 24.