Dermatopathia pigmentosa reticularis: a rare case

Nidhin Varghese, J. Prathibha
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引用次数: 0

Abstract

Dermatopathia pigmentosa reticularis (DPR) is a rare ectodermal dysplasia with a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. We report a case of a 21-year-old man who had generalized reticulate pigmentation, diffuse noncicatricial alopecia, and onychodystrophy of finger and toe nails. Along with this triad, he also had mild atrophy of skin over hands and feet, palms and soles, and loss of dermatoglyphics. There was no evidence of involvement of other organs with ectodermal origin.
网状色素性皮肤病1例
网状色素沉着性皮肤病(DPR)是一种罕见的外胚层发育不良,伴有全身性网状色素沉着、非瘢痕性脱发和甲营养不良。我们报告一例21岁的男性,他有广泛性网状色素沉着,弥漫性非瘢痕性脱发,以及手指和脚趾趾甲营养不良。除了这三种症状外,他还出现了手脚、手掌和脚底的皮肤轻度萎缩,以及皮肤印记的丧失。没有证据表明其他起源于外胚层的器官受累。
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19
审稿时长
27 weeks
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