斑纹毛囊性角化病:一种新的观察

H. Elmahi, S. Elloudi, S. Gallouj, F. Mernissi, M. Rimani
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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。
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.
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