• 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

1型神经纤维瘤病患者的Lisch结节特征

Characteristics of Lisch nodules in patients with neurofibromatosis type 1.

作者信息

Nichols John C, Amato Josh E, Chung Sophia M

机构信息

Department of Ophthalmology, University of Arizona, College of Medicine, Tucson, Arizona, USA.

出版信息

J Pediatr Ophthalmol Strabismus. 2003 Sep-Oct;40(5):293-6. doi: 10.3928/0191-3913-20030901-11.

DOI:10.3928/0191-3913-20030901-11
PMID:14560838
Abstract

PURPOSE

To assess the prevalence and location of Lisch nodules among patients with neurofibromatosis type 1.

PATIENTS AND METHODS

This was a prospective observational case series in which 369 consecutive patients from a neurofibromatosis clinic participated. Predetermined inclusion and exclusion criteria were applied to these participants. The presence of Lisch nodules was determined by one of the authors (SMC). The percentage of patients with neurofibromatosis type 1 with Lisch nodules was calculated. Lisch nodules were characterized as being distributed superiorly, inferiorly, or equally in each eye. The percentage of eyes in each group was ascertained.

RESULTS

Among patients of all ages with neurofibromatosis type 1, 63.2% had Lisch nodules, whereas 92% of postpubertal patients had Lisch nodules. Among eyes with Lisch nodules, 80% had an inferior distribution.

CONCLUSIONS

This study corroborated previously reported data regarding the prevalence of Lisch nodules in patients with neurofibromatosis type 1 and found that Lisch nodules were predominantly located inferiorly on the iris. The authors propose that exposure to sunlight may be the mechanism for this distribution of hamartomatous nodules.

摘要

目的

评估1型神经纤维瘤病患者中Lisch结节的患病率及位置。

患者与方法

这是一项前瞻性观察性病例系列研究,来自神经纤维瘤病诊所的369例连续患者参与其中。对这些参与者应用了预定的纳入和排除标准。Lisch结节的存在由作者之一(SMC)确定。计算1型神经纤维瘤病患者中存在Lisch结节的百分比。Lisch结节的特征为在每只眼中分布于上方、下方或均等分布。确定每组眼中的百分比。

结果

在所有年龄段的1型神经纤维瘤病患者中,63.2%有Lisch结节,而青春期后患者中有92%有Lisch结节。在有Lisch结节的眼中,80%分布于下方。

结论

本研究证实了先前报道的关于1型神经纤维瘤病患者中Lisch结节患病率的数据,并发现Lisch结节主要位于虹膜下方。作者提出,暴露于阳光下可能是错构瘤结节这种分布的机制。

相似文献

1
Characteristics of Lisch nodules in patients with neurofibromatosis type 1.1型神经纤维瘤病患者的Lisch结节特征
J Pediatr Ophthalmol Strabismus. 2003 Sep-Oct;40(5):293-6. doi: 10.3928/0191-3913-20030901-11.
2
A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1.对1型神经纤维瘤病成年患者中Lisch结节的负担和分布进行定量评估。
Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5035-43. doi: 10.1167/iovs.09-3650. Epub 2009 Jun 10.
3
Lisch nodules in neurofibromatosis type 2. Case report.2型神经纤维瘤病中的Lisch结节。病例报告。
Arch Ophthalmol. 1989 Nov;107(11):1571-2. doi: 10.1001/archopht.1989.01070020649012.
4
Lisch nodules in neurofibromatosis type 1.1型神经纤维瘤病中的Lisch结节
N Engl J Med. 1991 May 2;324(18):1264-6. doi: 10.1056/NEJM199105023241807.
5
Images of Lisch nodules across the spectrum.不同类型的Lisch结节图像。
Eye (Lond). 1993;7 ( Pt 1):95-101. doi: 10.1038/eye.1993.20.
6
Eye disorders in neurofibromatosis (NF1).神经纤维瘤病1型(NF1)中的眼部疾病
Coll Antropol. 2005;29 Suppl 1:29-31.
7
[Lisch nodules. Markers for a non-invasive diagnosis in Recklinghausen neurofibromatosis].[Lisch结节。用于神经纤维瘤病1型无创诊断的标志物]
Oftalmologia. 2008;52(4):56-61.
8
[Lisch nodules: an ophthalmic marker of neurofibromatosis type 1].[虹膜错构瘤:1型神经纤维瘤病的眼部标志物]
Pan Afr Med J. 2022 Jun 9;42:108. doi: 10.11604/pamj.2022.42.108.35079. eCollection 2022.
9
[Lisch nodule in neurofibromatosis type 1].[1型神经纤维瘤病中的Lisch结节]
Pan Afr Med J. 2017 Jul 21;27:218. doi: 10.11604/pamj.2017.27.218.11517. eCollection 2017.
10
Unilateral Lisch nodules in the absence of other features of neurofibromatosis 1.无神经纤维瘤病1型其他特征的单侧Lisch结节
Am J Ophthalmol. 2003 Apr;135(4):567-8. doi: 10.1016/s0002-9394(02)01974-8.

引用本文的文献

1
Novel Variants and Clinical Characteristics of 16 Patients from Southeast Asia with Genetic Variants in Neurofibromin-1.16例东南亚神经纤维瘤蛋白-1基因变异患者的新型变异及临床特征
J Pediatr Genet. 2021 Oct 19;12(2):135-140. doi: 10.1055/s-0041-1736457. eCollection 2023 Jun.
2
Ophthalmological assessment of children with neurofibromatosis type 1.神经纤维瘤病 1 型患儿的眼科评估。
Eur J Pediatr. 2013 Oct;172(10):1327-33. doi: 10.1007/s00431-013-2035-2. Epub 2013 May 25.
3
Don't it make my blue eyes brown: heterochromia and other abnormalities of the iris.
难道这不会使我的蓝眼睛变成棕色吗:虹膜异色症和其他虹膜异常。
Eye (Lond). 2012 Jan;26(1):29-50. doi: 10.1038/eye.2011.228. Epub 2011 Oct 7.
4
A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1.对1型神经纤维瘤病成年患者中Lisch结节的负担和分布进行定量评估。
Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5035-43. doi: 10.1167/iovs.09-3650. Epub 2009 Jun 10.
5
Unidentified bright objects on brain MRI in children as a diagnostic criterion for neurofibromatosis type 1.儿童脑部磁共振成像上不明的明亮物体作为1型神经纤维瘤病的诊断标准。
Pediatr Radiol. 2008 Mar;38(3):305-10. doi: 10.1007/s00247-007-0712-x. Epub 2008 Jan 30.
6
Quantification and anatomic distribution of choroidal abnormalities in patients with type I neurofibromatosis.I型神经纤维瘤病患者脉络膜异常的定量分析及解剖分布
Graefes Arch Clin Exp Ophthalmol. 2005 Oct;243(10):980-4. doi: 10.1007/s00417-005-1184-z. Epub 2005 Oct 20.
7
Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications.VHL和NF 1的眼科表现:病理及诊断意义
Fam Cancer. 2005;4(1):43-7. doi: 10.1007/s10689-004-1327-0.