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网状色素沉着性疾病的临床重叠：三例病例研究

Clinical Overlaps in Reticulate Pigmentary Disorders: A Study of Three Cases.

作者信息

Malik Nishtha, Nair Rahul S, Reddy Aravind, Chaurasia Pooja, Pillai Niranjana S

机构信息

Dermatology, Venereology, and Leprosy, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune (Deemed to be University), Pune, IND.

Orthopedic Surgery, Holy Cross Hospital, Kollam, IND.

出版信息

Cureus. 2024 Mar 20;16(3):e56600. doi: 10.7759/cureus.56600. eCollection 2024 Mar.

DOI:10.7759/cureus.56600
PMID:38646262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11031628/
Abstract

Reticulate pigmentary disorders are autosomal dominant pigmentary disorders caused by abnormalities in the keratin 5 and keratin 14 genes. Here, we report three cases of reticulate hyperpigmentation disorders with clinical overlaps of the reticulate acropigmentation of Kitamura, Dowling-Degos disease (DDD), and dyschromatosis symmetrica hereditaria (DSH), all three having limited treatment options.

摘要

网状色素沉着障碍是由角蛋白5和角蛋白14基因异常引起的常染色体显性色素沉着障碍。在此，我们报告3例网状色素沉着过度性疾病，其临床表现与北村网状肢端色素沉着症、Dowling-Degos病（DDD）和遗传性对称性色素异常症（DSH）有重叠，这三种疾病的治疗选择均有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/fcfcb0ac3c74/cureus-0016-00000056600-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/25705dc88711/cureus-0016-00000056600-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/10692489a488/cureus-0016-00000056600-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/d87460175fe6/cureus-0016-00000056600-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/d162a8c4048d/cureus-0016-00000056600-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/9fed8e9c69ad/cureus-0016-00000056600-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/fcfcb0ac3c74/cureus-0016-00000056600-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/25705dc88711/cureus-0016-00000056600-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/10692489a488/cureus-0016-00000056600-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/d87460175fe6/cureus-0016-00000056600-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/d162a8c4048d/cureus-0016-00000056600-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/9fed8e9c69ad/cureus-0016-00000056600-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a0/11031628/fcfcb0ac3c74/cureus-0016-00000056600-i06.jpg

相似文献

1
Clinical Overlaps in Reticulate Pigmentary Disorders: A Study of Three Cases.网状色素沉着性疾病的临床重叠：三例病例研究
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Inherited Reticulate Pigmentary Disorders.遗传性网状色素沉着障碍。
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Dyschromatosis symmetrica hereditaria and reticulate acropigmentation of Kitamura: An update.遗传性对称性色素异常症和 Kitamura 网状肢端色素沉着：更新。
J Dermatol Sci. 2019 Feb;93(2):75-81. doi: 10.1016/j.jdermsci.2019.01.004. Epub 2019 Jan 15.
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A case of reticulate acropigmentation of kitamura: dowling degos disease overlap with unusual clinical manifestations.一例北村网状肢端色素沉着症：与多林-德戈斯病重叠且有不寻常临床表现
Indian J Dermatol. 2014 May;59(3):290-2. doi: 10.4103/0019-5154.131408.
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本文引用的文献

1
A case of reticulate acropigmentation of kitamura: dowling degos disease overlap with unusual clinical manifestations.一例北村网状肢端色素沉着症：与多林-德戈斯病重叠且有不寻常临床表现
Indian J Dermatol. 2014 May;59(3):290-2. doi: 10.4103/0019-5154.131408.
2
Dyschromatosis symmetrica hereditaria of late onset?迟发性对称性遗传性色素异常症？
Case Rep Dermatol Med. 2014;2014:639537. doi: 10.1155/2014/639537. Epub 2014 Feb 4.
3
Reticulate pigmentary disorders.网状色素紊乱。
Indian J Dermatol Venereol Leprol. 2013 Jan-Feb;79(1):17-29. doi: 10.4103/0378-6323.104665.