唐氏综合征伴穿孔毛囊炎一例罕见病例报告

IF 0.2 Q4 DERMATOLOGY
Aswath Rajan, V. Pai, P. Shukla
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引用次数: 1

摘要

穿孔性毛囊炎是一种原发性穿孔性疾病,其特征是经表皮消除现象。它与各种疾病有关,如银屑病、青少年黑棘皮病、糖尿病、肾衰竭、心力衰竭和恶性肿瘤。其他原发性穿孔性皮肤病有Kyrle病、反应性穿孔性胶原病和穿孔性serpiginosa弹性病。在穿孔性皮肤病与遗传性疾病(如唐氏综合征)的相关性中,有穿孔性弹性蛋白病和极少数反应性穿孔性胶原病的报道。我们报告了第一例11岁男孩,他是已知的唐氏综合征病例,表现为穿透性毛囊炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perforating folliculitis in Down’s syndrome − a rare case report
Perforating folliculitis is a primary perforating disorder, characterized by the phenomenon of transepidermal elimination. It is associated with various disorders such as psoriasis, juvenile acanthosis nigricans, diabetic mellitus, renal failure, cardiac failure, and malignant neoplasia. Other primary perforating dermatoses are Kyrle’s disease, reactive perforating collagenosis, and elastosis perforans serpiginosa. Among the association of perforating dermatoses with genetic diseases like Down’s syndrome, elastosis perforans serpiginosa and very rarely reactive perforating collagenosis have been reported. We report the first case of an 11-year-old boy who is a known case of Down syndrome presented with perforating folliculitis.
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