多形性红斑合并苔藓样粘膜炎1例

{"title":"多形性红斑合并苔藓样粘膜炎1例","authors":"","doi":"10.36879/jcmi.20.000124","DOIUrl":null,"url":null,"abstract":"Erythema multiforme (EM) is an acute, self-limiting, mucocutaneous disease. While the histopathologic and immunopathologic\nfeature of EM is not highly specific, the diagnosis is mainly based on the etiology and clinical manifestations. This report presented\na patient whose clinical investigation indicated EM while histopathology suggested lichenoid mucositis. Considering the classic oral\nand skin presentation matching EM, as well as the acute onsite and spontaneous resolution of the lesions, the diagnosis highly favored\nEM. The immunofluorescent findings might suggest a potential common pathologic process on EM and lichenoid mucositis, which\nrequires further investigation.","PeriodicalId":91401,"journal":{"name":"SM journal of clinical and medical imaging","volume":"10 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Erythema multiforme complicated with lichenoid mucositis: A case report\",\"authors\":\"\",\"doi\":\"10.36879/jcmi.20.000124\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Erythema multiforme (EM) is an acute, self-limiting, mucocutaneous disease. While the histopathologic and immunopathologic\\nfeature of EM is not highly specific, the diagnosis is mainly based on the etiology and clinical manifestations. This report presented\\na patient whose clinical investigation indicated EM while histopathology suggested lichenoid mucositis. Considering the classic oral\\nand skin presentation matching EM, as well as the acute onsite and spontaneous resolution of the lesions, the diagnosis highly favored\\nEM. The immunofluorescent findings might suggest a potential common pathologic process on EM and lichenoid mucositis, which\\nrequires further investigation.\",\"PeriodicalId\":91401,\"journal\":{\"name\":\"SM journal of clinical and medical imaging\",\"volume\":\"10 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-08-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"SM journal of clinical and medical imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36879/jcmi.20.000124\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"SM journal of clinical and medical imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36879/jcmi.20.000124","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

多形性红斑(EM)是一种急性,自限性,皮肤粘膜疾病。而EM的组织病理和免疫病理特征特异性不高,诊断主要基于病因和临床表现。本报告报告了一位临床调查显示EM而组织病理学提示地衣样粘膜炎的患者。考虑到经典的口腔和皮肤表现与EM相匹配,以及病变的急性现场和自发消退,诊断高度倾向于dem。免疫荧光结果可能提示EM和苔藓样粘膜炎的潜在共同病理过程,这需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Erythema multiforme complicated with lichenoid mucositis: A case report
Erythema multiforme (EM) is an acute, self-limiting, mucocutaneous disease. While the histopathologic and immunopathologic feature of EM is not highly specific, the diagnosis is mainly based on the etiology and clinical manifestations. This report presented a patient whose clinical investigation indicated EM while histopathology suggested lichenoid mucositis. Considering the classic oral and skin presentation matching EM, as well as the acute onsite and spontaneous resolution of the lesions, the diagnosis highly favored EM. The immunofluorescent findings might suggest a potential common pathologic process on EM and lichenoid mucositis, which requires further investigation.
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
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信