• 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

伴有黏膜受累的格雷厄姆-利特尔-皮卡迪-拉叙厄尔综合征：1例罕见病例

Graham-Little-Piccardi-Lassueur Syndrome with Mucosal Involvement: A Rare Case.

作者信息

Polra Rutoo Vipulkumar, Tandel Jinal Jainendrabhai, Nair Pragya Ashok

机构信息

Department of Dermatology, Shree Krishna Hospital, Bhaikaka University, Karamsad, Gujarat, India.

Dina Skin Care, Surat, Gujarat, India.

出版信息

Int J Trichology. 2023 Nov-Dec;15(6):251-254. doi: 10.4103/ijt.ijt_88_22. Epub 2024 Oct 7.

DOI:10.4103/ijt.ijt_88_22
PMID:39600425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11588195/
Abstract

Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a type of lichen planopilaris. It mainly affects females aged 40-60 years. It is characterized by the triad of patchy cicatricial alopecia of the scalp, noncicatricial alopecia of the axilla and groin and a follicular spinous papule on the body, scalp, or both. The diagnosis is based on clinicopathological correlation. Different modalities of treatment are available with unsatisfactory responses, so early diagnosis is necessary to prevent progression and scarring alopecia. A case of GLPLS with classical features on clinical, dermoscopic, and histopathological examination is presented in a 73-year-old female.

摘要

格雷厄姆-利特尔-皮卡迪-拉叙厄尔综合征（GLPLS）是扁平苔藓样毛发角化病的一种类型。它主要影响40至60岁的女性。其特征为头皮瘢痕性斑秃、腋窝和腹股沟非瘢痕性脱发以及身体、头皮或两者上的毛囊棘状丘疹三联征。诊断基于临床病理相关性。虽有不同的治疗方式，但反应不尽人意，因此早期诊断对于预防病情进展和瘢痕性脱发很有必要。本文报告了一例73岁女性患者，其在临床、皮肤镜和组织病理学检查中具有GLPLS的典型特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/e0ff6a3bc48c/IJT-15-251-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/aa52cedbc59f/IJT-15-251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/e36f4ce6a1f5/IJT-15-251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/6139e9b92a8c/IJT-15-251-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/c98af54c3380/IJT-15-251-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/b4d92437dd65/IJT-15-251-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/fdd1de6c69b3/IJT-15-251-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/e0ff6a3bc48c/IJT-15-251-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/aa52cedbc59f/IJT-15-251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/e36f4ce6a1f5/IJT-15-251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/6139e9b92a8c/IJT-15-251-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/c98af54c3380/IJT-15-251-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/b4d92437dd65/IJT-15-251-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/fdd1de6c69b3/IJT-15-251-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c604/11588195/e0ff6a3bc48c/IJT-15-251-g007.jpg

相似文献

1
Graham-Little-Piccardi-Lassueur Syndrome with Mucosal Involvement: A Rare Case.伴有黏膜受累的格雷厄姆-利特尔-皮卡迪-拉叙厄尔综合征：1例罕见病例
Int J Trichology. 2023 Nov-Dec;15(6):251-254. doi: 10.4103/ijt.ijt_88_22. Epub 2024 Oct 7.
2
Graham-Little Piccardi Lassueur syndrome and review of the literature.格雷厄姆-利特尔-皮卡迪-拉叙厄尔综合征及文献综述
Clin Case Rep. 2021 Sep 5;9(9):e04761. doi: 10.1002/ccr3.4761. eCollection 2021 Sep.
3
Graham-little piccardi lassueur syndrome: an unusual variant of follicular lichen planus.格雷厄姆-利特尔-皮卡迪-拉叙厄尔综合征：毛囊扁平苔藓的一种罕见变体。
Int J Trichology. 2011 Jan;3(1):28-30. doi: 10.4103/0974-7753.82129.
4
Clinical, Dermoscopic and In-Vivo Reflectance Confocal Microscopy Evaluation of a Case of Graham Little-Piccardi-Lassueur Syndrome Successfully Treated with Narrowband-UVB Phototherapy.窄带紫外线B光疗成功治疗一例格雷厄姆·利特尔-皮卡迪-拉叙厄尔综合征的临床、皮肤镜及活体反射式共聚焦显微镜评估
Dermatol Ther (Heidelb). 2020 Aug;10(4):887-892. doi: 10.1007/s13555-020-00410-x. Epub 2020 Jun 12.
5
Graham-Little-Piccardi-Lassueur syndrome.格雷厄姆-利特尔-皮卡迪-拉叙厄尔综合征
Dermatol Online J. 2011 Oct 15;17(10):30.
6
Pediatric case of Graham Little Piccardi Lassueur syndrome - A rare entity.小儿格雷厄姆·利特尔-皮卡迪-拉叙厄尔综合征病例——一种罕见病症。
Drug Discov Ther. 2019 Nov 14;13(5):294-296. doi: 10.5582/ddt.2019.01055. Epub 2019 Oct 27.
7
A case of Graham-Little-Piccardi-Lasseur syndrome.一例格雷厄姆-利特尔-皮卡迪-拉叙尔综合征病例。
Dermatol Online J. 2015 Jun 16;21(6):13030/qt7gj157xg.
8
Lassueur-Graham-Little-Piccardi syndrome.拉叙厄尔-格雷厄姆-利特尔-皮卡迪综合征
Dermatol Online J. 2007 Jan 27;13(1):12.
9
Lichen planopilaris epidemiology: a retrospective study of 80 cases.扁平苔藓样毛发角化病的流行病学：一项对80例病例的回顾性研究。
An Bras Dermatol. 2015 Sep-Oct;90(5):666-70. doi: 10.1590/abd1806-4841.20153923.
10
Graham little piccardi lasseur syndrome: a rare case report with concomitant hypertrophic lichen planus.格雷厄姆·利特尔-皮卡迪-拉瑟尔综合征：一例合并肥厚性扁平苔藓的罕见病例报告。
Int J Trichology. 2013 Oct;5(4):199-200. doi: 10.4103/0974-7753.130403.