斑纹毛囊性角化病:一种新的观察

H. Elmahi, S. Elloudi, S. Gallouj, F. Mernissi, M. Rimani
{"title":"斑纹毛囊性角化病:一种新的观察","authors":"H. Elmahi, S. Elloudi, S. Gallouj, F. Mernissi, M. Rimani","doi":"10.19070/2332-2977-1700027","DOIUrl":null,"url":null,"abstract":"Scarring alopecia in association with follicular hyperkeratosis is the primary characteristic of keratosis pilaris atrophicans (KPA). It affects mainly the face and scalp and can be inflammatory in nature [1]. Widespread KP can also be seen. keratosis pilaris atrophicans is a group of cutaneous disorders that may represent a spectrum of 1 disease. Differences in localization and the degree of inflammation and atrophy have been used to distinguish these various disorders [1]. They are genetic disorders with different modes of inheritance. Heterogeneity in the mode of inheritance exists not only between different types of KPA but also within 1 type, such as keratosis follicularis spinulosa decalvans (KFSD) [1, 2]. The pathogenesis is not known, but abnormal follicular keratinization has been suggested.","PeriodicalId":15418,"journal":{"name":"Journal of Clinical Dermatology","volume":"2 1","pages":"107-109"},"PeriodicalIF":0.0000,"publicationDate":"2017-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Keratosis Follicularis Spinulosa Decalvans: A New Observation\",\"authors\":\"H. Elmahi, S. Elloudi, S. Gallouj, F. Mernissi, M. Rimani\",\"doi\":\"10.19070/2332-2977-1700027\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Scarring alopecia in association with follicular hyperkeratosis is the primary characteristic of keratosis pilaris atrophicans (KPA). It affects mainly the face and scalp and can be inflammatory in nature [1]. Widespread KP can also be seen. keratosis pilaris atrophicans is a group of cutaneous disorders that may represent a spectrum of 1 disease. Differences in localization and the degree of inflammation and atrophy have been used to distinguish these various disorders [1]. They are genetic disorders with different modes of inheritance. Heterogeneity in the mode of inheritance exists not only between different types of KPA but also within 1 type, such as keratosis follicularis spinulosa decalvans (KFSD) [1, 2]. The pathogenesis is not known, but abnormal follicular keratinization has been suggested.\",\"PeriodicalId\":15418,\"journal\":{\"name\":\"Journal of Clinical Dermatology\",\"volume\":\"2 1\",\"pages\":\"107-109\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Dermatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.19070/2332-2977-1700027\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Dermatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.19070/2332-2977-1700027","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

与毛囊性角化过度相关的瘢痕性脱发是萎缩性角化病(KPA)的主要特征。它主要影响面部和头皮,本质上可能是炎症[1]。广泛的KP也可以看到。萎缩性角化病是一组皮肤疾病,可能代表一种疾病的谱。不同部位以及炎症和萎缩程度的差异已被用来区分这些不同的疾病[1]。它们是遗传方式不同的遗传病。遗传方式的异质性不仅存在于KPA的不同类型之间,也存在于同一类型内,如毛囊性棘状角化病(KFSD)[1,2]。发病机制尚不清楚,但异常滤泡角化已提出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Keratosis Follicularis Spinulosa Decalvans: A New Observation
Scarring alopecia in association with follicular hyperkeratosis is the primary characteristic of keratosis pilaris atrophicans (KPA). It affects mainly the face and scalp and can be inflammatory in nature [1]. Widespread KP can also be seen. keratosis pilaris atrophicans is a group of cutaneous disorders that may represent a spectrum of 1 disease. Differences in localization and the degree of inflammation and atrophy have been used to distinguish these various disorders [1]. They are genetic disorders with different modes of inheritance. Heterogeneity in the mode of inheritance exists not only between different types of KPA but also within 1 type, such as keratosis follicularis spinulosa decalvans (KFSD) [1, 2]. The pathogenesis is not known, but abnormal follicular keratinization has been suggested.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Impacts of Acupuncture Therapy on Herpes Zoster: Report of 3 Cases Leukemia Cutis in a Patient with Metastatic Pancreatic Cancer: A Case Report Dermatologic Manifestation Of COVID-19: Review Of Case Series Dupilumab: Friend or Foe to Alopecia Areata? A Review Of Erythroid Differentiation Regulator 1 (ERDR1) As A Therapeutic Target In Skin Inflammation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1