Endogenous ochronosis with keratoelastoidosis marginalis

R. Mythreyi, Adikrishnan Swaminathan, A. Priyadarshini, S. Rangarajan, S. Murugan
{"title":"Endogenous ochronosis with keratoelastoidosis marginalis","authors":"R. Mythreyi, Adikrishnan Swaminathan, A. Priyadarshini, S. Rangarajan, S. Murugan","doi":"10.4103/ijdpdd.ijdpdd_50_18","DOIUrl":null,"url":null,"abstract":"Endogenous ochronosis is a manifestation of alkaptonuria, a rare metabolic disease due to homogentisic acid oxidase deficiency. Darkened urine and arthropathy are the other two components that complete the triad of alkaptonuria. Pigmentation of skin, the presenting feature, is common over the face and ears. A few cases of pigmentation of the palms and soles are reported. Here, we report a case of endogenous ochronosis presenting as keratoelastoidosis marginalis, which is a rare manifestation.","PeriodicalId":423971,"journal":{"name":"Indian Journal of Dermatopathology and Diagnostic Dermatology","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Dermatopathology and Diagnostic Dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijdpdd.ijdpdd_50_18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Endogenous ochronosis is a manifestation of alkaptonuria, a rare metabolic disease due to homogentisic acid oxidase deficiency. Darkened urine and arthropathy are the other two components that complete the triad of alkaptonuria. Pigmentation of skin, the presenting feature, is common over the face and ears. A few cases of pigmentation of the palms and soles are reported. Here, we report a case of endogenous ochronosis presenting as keratoelastoidosis marginalis, which is a rare manifestation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
内源性衰老伴边缘角弹性样变性
内源性衰老症是由均质酸氧化酶缺乏症引起的罕见代谢性疾病——尿酸尿症的一种表现。尿变黑和关节病是完成尿黑尿三征的另外两个组成部分。色素沉着的皮肤,呈现特征,是常见的在脸和耳朵。报告了手掌和脚底色素沉着的少数病例。在此,我们报告一例内源性衰老,表现为边缘角弹性样变性,这是一种罕见的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Cauliflower-like growth at an unusual site: A clinical diagnostic dilemma Blaschko-linear Becker’s naevus over lower limb: A case study and literature review Endogenous ochronosis/Alkaptonuria: A case report highlighting the correlation between dermoscopy and histopathology Amelanotic metastatic dermal melanoma with an unknown primary: A double diagnostic dilemma Adding insult to injury: Fatal rhino-orbital mucormycosis eventuating in cutaneous involvement post-SARS-COV2 infection in a young female
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1