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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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/c3097e1045a9/omaa079f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/a00bbdec31d0/omaa079f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/cc9d31b9712d/omaa079f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/d8cae2037541/omaa079f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/27a3c48f68ab/omaa079f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/3f0203dceae5/omaa079f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/4ae1ae063efe/omaa079f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/d2d73cf150f3/omaa079f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/c846b4c7109d/omaa079f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/7118fb79a9bd/omaa079f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/c3097e1045a9/omaa079f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/a00bbdec31d0/omaa079f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/cc9d31b9712d/omaa079f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/d8cae2037541/omaa079f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/27a3c48f68ab/omaa079f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/3f0203dceae5/omaa079f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/4ae1ae063efe/omaa079f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/d2d73cf150f3/omaa079f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/c846b4c7109d/omaa079f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/7118fb79a9bd/omaa079f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a00/7507869/c3097e1045a9/omaa079f10.jpg

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本文引用的文献

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Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant.内格利-弗朗切斯科蒂-雅达松综合征与网状色素性皮病：同一KRT14移码变异患者家系内的表型重叠
Br J Dermatol. 2019 Oct;181(4):864-866. doi: 10.1111/bjd.17997. Epub 2019 Jul 15.
2
Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder.网状色素性皮病：一种罕见的网状色素沉着性疾病。
Indian Dermatol Online J. 2013 Jan;4(1):40-2. doi: 10.4103/2229-5178.105470.
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Dyschromatosis universalis hereditaria.
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[Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis. Two allelic ectodermal dysplasias related to mutations of dominant gene coding for keratin 14].[内格利-弗朗切斯科蒂-雅达松综合征与网状色素沉着性皮病。两种与编码角蛋白14的显性基因突变相关的等位基因外胚层发育异常]
Ann Dermatol Venereol. 2007 Jun-Jul;134(6-7):595. doi: 10.1016/s0151-9638(07)89283-0.
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Reticulate hyperpigmentation.网状色素沉着。
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Dermatopathia pigmentosa reticularis.
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Dermatopathia pigmentosa reticularis: a report of a family demonstrating autosomal dominant inheritance.网状色素性皮病：一个显示常染色体显性遗传的家系报告。
J Am Acad Dermatol. 1992 Feb;26(2 Pt 2):298-301. doi: 10.1016/0190-9622(92)70039-i.