Stasis dermatitis and pigmented purpuric dermatoses: Histological characterization and review of literature

M. S. Hoffet, D. L. Perruchoud, K. Gadaldi, K. Heidemeyer, S. Bossart, L. Borradori, A. A. Ramelet, L. Feldmeyer
{"title":"Stasis dermatitis and pigmented purpuric dermatoses: Histological characterization and review of literature","authors":"M. S. Hoffet,&nbsp;D. L. Perruchoud,&nbsp;K. Gadaldi,&nbsp;K. Heidemeyer,&nbsp;S. Bossart,&nbsp;L. Borradori,&nbsp;A. A. Ramelet,&nbsp;L. Feldmeyer","doi":"10.1002/jvc2.569","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Stasis dermatitis and pigmented purpuric dermatoses can both manifest as hyperpigmentation, petechiae and/or purpura on the lower extremities, posing a challenge for macroscopic differentiation. We investigated the histological differences in these two conditions.</p>\n </section>\n \n <section>\n \n <h3> Objectives</h3>\n \n <p>To determine the histological characteristics of stasis dermatitis and pigmented purpuric dermatosis.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Skin biopsy specimens were obtained from seven patients with stasis dermatitis, 15 with pigmented purpuric dermatosis, and three control patients. The samples were analysed for histological changes (hematoxylin-eosin), melanin (silver nitrate), iron, elastic stain, and with an immunohistochemistry for melanocytes (Melan-A).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The predominant histological features of stasis dermatitis were hemosiderin deposits, eosinophils and telangiectasias. Pigmented purpuric dermatosis was characterized by extensive erythrocyte extravasation, interface changes and spongiosis.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>The distinct histological characteristics of stasis dermatitis and pigmented purpuric dermatosis can improve the diagnostic classification of these entities.</p>\n </section>\n </div>","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"4 1","pages":"166-173"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.569","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JEADV clinical practice","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jvc2.569","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Stasis dermatitis and pigmented purpuric dermatoses can both manifest as hyperpigmentation, petechiae and/or purpura on the lower extremities, posing a challenge for macroscopic differentiation. We investigated the histological differences in these two conditions.

Objectives

To determine the histological characteristics of stasis dermatitis and pigmented purpuric dermatosis.

Methods

Skin biopsy specimens were obtained from seven patients with stasis dermatitis, 15 with pigmented purpuric dermatosis, and three control patients. The samples were analysed for histological changes (hematoxylin-eosin), melanin (silver nitrate), iron, elastic stain, and with an immunohistochemistry for melanocytes (Melan-A).

Results

The predominant histological features of stasis dermatitis were hemosiderin deposits, eosinophils and telangiectasias. Pigmented purpuric dermatosis was characterized by extensive erythrocyte extravasation, interface changes and spongiosis.

Conclusions

The distinct histological characteristics of stasis dermatitis and pigmented purpuric dermatosis can improve the diagnostic classification of these entities.

Abstract Image

背景 瘀积性皮炎和色素性紫癜性皮肤病均可表现为下肢色素沉着、瘀斑和/或紫癜,这给宏观鉴别带来了挑战。我们对这两种疾病的组织学差异进行了研究。 目的 确定瘀积性皮炎和色素性紫癜性皮肤病的组织学特征。 方法 从 7 名瘀积性皮炎患者、15 名色素性紫癜皮病患者和 3 名对照组患者身上获取皮肤活检标本。对标本进行组织学变化(苏木精-伊红)、黑色素(硝酸银)、铁、弹性染色和黑色素细胞免疫组化(Melan-A)分析。 结果 瘀积性皮炎的主要组织学特征是血色素沉积、嗜酸性粒细胞和毛细血管扩张。色素性紫癜性皮炎的特点是广泛的红细胞外渗、界面变化和海绵状增生。 结论 瘀积性皮炎和色素性紫癜皮肤病的不同组织学特征可改进对这些实体的诊断分类。
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
0.30
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