Laugier-Hunziker综合征，老年人

Q4 Medicine Atencion Primaria Practica Pub Date : 2022-04-01 DOI:10.1016/j.appr.2022.100130

Juan Sebastian Theran León , Laura Yibeth Esteban Badillo , Luis Andres Dulcey

{"title":"Laugier-Hunziker综合征，老年人","authors":"Juan Sebastian Theran León , Laura Yibeth Esteban Badillo , Luis Andres Dulcey","doi":"10.1016/j.appr.2022.100130","DOIUrl":null,"url":null,"abstract":"<div><p>Laugier-Hunziker syndrome (LHS) is a rare benign disorder, often acquired in adulthood, characterized by lentiginous hyperpigmentation of the oral mucosa and lips, associated with longitudinal melanonychia. Its importance is based on the early recognition and differential diagnosis of various oral and cutaneous hyperpigmentation pathologies. The case of a 74-year-old man with probable SLH is presented below and important differential diagnoses are discussed.</p></div>","PeriodicalId":52231,"journal":{"name":"Atencion Primaria Practica","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2605073022000074/pdfft?md5=48504f21262f50cb4b0c9f5c32550c90&pid=1-s2.0-S2605073022000074-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Síndrome Laugier-Hunziker, en el adulto mayor\",\"authors\":\"Juan Sebastian Theran León , Laura Yibeth Esteban Badillo , Luis Andres Dulcey\",\"doi\":\"10.1016/j.appr.2022.100130\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Laugier-Hunziker syndrome (LHS) is a rare benign disorder, often acquired in adulthood, characterized by lentiginous hyperpigmentation of the oral mucosa and lips, associated with longitudinal melanonychia. Its importance is based on the early recognition and differential diagnosis of various oral and cutaneous hyperpigmentation pathologies. The case of a 74-year-old man with probable SLH is presented below and important differential diagnoses are discussed.</p></div>\",\"PeriodicalId\":52231,\"journal\":{\"name\":\"Atencion Primaria Practica\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2605073022000074/pdfft?md5=48504f21262f50cb4b0c9f5c32550c90&pid=1-s2.0-S2605073022000074-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atencion Primaria Practica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2605073022000074\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atencion Primaria Practica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2605073022000074","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}

引用次数: 0

摘要

Laugier-Hunziker综合征(LHS)是一种罕见的良性疾病，通常在成年期获得，其特征是口腔黏膜和嘴唇的黄斑性色素沉着，并伴有纵向黑甲癣。它的重要性在于对各种口腔和皮肤色素沉着病的早期识别和鉴别诊断。以下是一例74岁男性SLH的病例，并讨论了重要的鉴别诊断。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

Síndrome Laugier-Hunziker, en el adulto mayor

Laugier-Hunziker syndrome (LHS) is a rare benign disorder, often acquired in adulthood, characterized by lentiginous hyperpigmentation of the oral mucosa and lips, associated with longitudinal melanonychia. Its importance is based on the early recognition and differential diagnosis of various oral and cutaneous hyperpigmentation pathologies. The case of a 74-year-old man with probable SLH is presented below and important differential diagnoses are discussed.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊