A case of patch granuloma annulare with CD68-negative, CD163-positive M2 macrophages infiltration in an interstitial pattern

IF 1.1 Q4 ALLERGY
Kenta Ikeda MD, Kazuko Mizuno MD, PhD, Osamu Yamasaki MD, PhD, Shin Morizane MD, PhD
{"title":"A case of patch granuloma annulare with CD68-negative, CD163-positive M2 macrophages infiltration in an interstitial pattern","authors":"Kenta Ikeda MD,&nbsp;Kazuko Mizuno MD, PhD,&nbsp;Osamu Yamasaki MD, PhD,&nbsp;Shin Morizane MD, PhD","doi":"10.1002/cia2.12260","DOIUrl":null,"url":null,"abstract":"<p>Patch granuloma annulare is a rare type of granuloma annulare. Histopathologically, patch granuloma annulare shows interstitial infiltration of histiocytes. In our case, immunohistochemical analyses demonstrated CD68-negative, CD163-positive M2 macrophages infiltration in an interstitial pattern.\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2022-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12260","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cutaneous Immunology and Allergy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cia2.12260","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

Abstract

Patch granuloma annulare is a rare type of granuloma annulare. Histopathologically, patch granuloma annulare shows interstitial infiltration of histiocytes. In our case, immunohistochemical analyses demonstrated CD68-negative, CD163-positive M2 macrophages infiltration in an interstitial pattern.

Abstract Image

环状斑块性肉芽肿伴CD68阴性、CD163阳性M2巨噬细胞间质浸润1例
环状斑块肉芽肿(GA)是一种罕见的肉芽肿类型,其特征是无症状和非特异性皮肤变色,进展缓慢在组织病理学上,斑块型GA表现为间质型,而经典型GA通常表现为栅栏型,两者在免疫组织化学上的表现不同在此,我们报告一例环状斑块性肉芽肿伴cd68阴性、cd163阳性M2巨噬细胞间质浸润。
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 求助全文
来源期刊
CiteScore
0.60
自引率
10.00%
发文量
69
审稿时长
12 weeks
×
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