Hazell M, Marks R
Br J Dermatol. 1984 Jul;111(1):101-9. doi: 10.1111/j.1365-2133.1984.tb04023.x.
We describe four patients with congenital follicular hyperkeratosis, of whom three also had pseudoacanthosis nigricans and two had facial abnormalities. Skin specimens were studied by light microscopy, autoradiography, histochemistry and scanning electron microscopy, and the results were compared with those from patients with keratosis pilaris. The condition appears to constitute a distinctive form of ichthyosis in which the abnormal epidermal differentiation occurs mainly within the hair follicles.
我们描述了4例先天性毛囊性角化过度患者,其中3例还患有假性黑棘皮病,2例有面部异常。通过光学显微镜、放射自显影、组织化学和扫描电子显微镜对皮肤标本进行了研究,并将结果与毛发角化病患者的结果进行了比较。这种情况似乎构成了一种独特的鱼鳞病形式,其中异常的表皮分化主要发生在毛囊内。