Keratosis Follicularis Spinulosa Decalvans: A New Observation

H. Elmahi, S. Elloudi, S. Gallouj, F. Mernissi, M. Rimani
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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.
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斑纹毛囊性角化病:一种新的观察
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。
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