伴有胡须脱发的网状色素性皮病：叙利亚的首例报告。

Dermatopathia pigmentosa reticularis with beard alopecia: first report from Syria.

作者信息

Elias Lama, Bleidy Rahaf, Hasan Foz, Romeah Abdalhalem, Houreih Mohammad Adib

机构信息

Dermatology Department, Tishreen University Hospital, Lattakia, Syria.

Pathology Department, Tishreen University Faculity of Medicine, Lattakia, Syria.

出版信息

Oxf Med Case Reports. 2020 Sep 22;2020(9):omaa079. doi: 10.1093/omcr/omaa079. eCollection 2020 Sep.

DOI:10.1093/omcr/omaa079

PMID:32995033

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7507869/

Abstract

Dermatopathia pigmentosa reticularis (DPR) is a rare disorder with characteristic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia and onychodystrophy. We report the first case from Syria with classical features of the triad along with hyperhidrosis and adermatoglyphia. Based on previous studies this case is distinguished by the location of alopecia on the beard which is not reported before and distinctive histopathological features were found on the biopsy.

摘要

网状色素沉着性皮病（DPR）是一种罕见的疾病，具有全身性网状色素沉着、非瘢痕性脱发和甲营养不良三联征这一特征。我们报告了叙利亚的首例具有该三联征典型特征以及多汗症和无指纹症的病例。根据以往研究，该病例的独特之处在于胡须部位出现脱发，此前未见报道，且活检发现了独特的组织病理学特征。