• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

特发性足底汗腺炎:一种主要发生于儿童的嗜中性小汗腺汗腺炎。

Idiopathic plantar hidradenitis: a neutrophilic eccrine hidradenitis occurring primarily in children.

作者信息

Stahr B J, Cooper P H, Caputo R V

机构信息

Department of Pathology, Emory University, Atlanta, GA.

出版信息

J Cutan Pathol. 1994 Aug;21(4):289-96. doi: 10.1111/j.1600-0560.1994.tb00702.x.

DOI:10.1111/j.1600-0560.1994.tb00702.x
PMID:7798384
Abstract

Neutrophilic eccrine hidradenitis (NEH) has been described in a variety of clinical settings but is most often seen in leukemic patients receiving chemotherapy. We have recently encountered 6 healthy individuals, of whom 5 were children, who developed NEH localized to the feet. The patients were from 9 to 21 years of age. The presenting complaint was rapid development of tenderness of the feet with varying degrees of morbidity. At clinical evaluation, tender, erythematous papules and nodules were confined to the feet, primarily the plantar surfaces. The major differential diagnoses were erythema nodosum and vasculitis. Laboratory studies were non-contributory. Histologically, the findings were generally similar to those of NEH with certain exceptions, most notably the absence of syringosquamous metaplasia and the presence, in most cases, of neutrophilic abscesses in eccrine coils. Inflammatory and degenerative changes involved primarily the eccrine duct (coiled and dermal), and tended to spare the secretory apparatus. Stains for microorganisms were negative. There were brief recurrences in some of the patients, but those followed over time have remained well. We suggest the term idiopathic plantar hidradenitis for this condition.

摘要

嗜中性小汗腺汗管炎(NEH)已在多种临床情况下被描述,但最常见于接受化疗的白血病患者。我们最近遇到了6名健康个体,其中5名是儿童,他们患上了局限于足部的NEH。这些患者年龄在9至21岁之间。主要症状是足部迅速出现压痛,并伴有不同程度的发病情况。临床评估时,压痛性红斑丘疹和结节局限于足部,主要在足底表面。主要的鉴别诊断是结节性红斑和血管炎。实验室检查无诊断价值。组织学上,其表现通常与NEH相似,但有某些例外,最显著的是没有汗腺鳞状化生,且在大多数情况下,汗腺螺旋管中有嗜中性脓肿。炎症和退行性改变主要累及汗腺导管(螺旋状和真皮内导管),而分泌装置往往未受影响。微生物染色为阴性。一些患者有短暂复发,但随着时间推移,他们都恢复良好。我们建议将这种情况称为特发性足底汗管炎。

相似文献

1
Idiopathic plantar hidradenitis: a neutrophilic eccrine hidradenitis occurring primarily in children.特发性足底汗腺炎:一种主要发生于儿童的嗜中性小汗腺汗腺炎。
J Cutan Pathol. 1994 Aug;21(4):289-96. doi: 10.1111/j.1600-0560.1994.tb00702.x.
2
Idiopathic palmoplantar hidradenitis.
Am J Dermatopathol. 1996 Aug;18(4):413-6. doi: 10.1097/00000372-199608000-00015.
3
Idiopathic plantar hidradenitis.特发性足底汗腺炎
J Eur Acad Dermatol Venereol. 1998 May;10(3):257-61.
4
Recurrent palmoplantar hidradenitis in children.
Arch Dermatol. 1995 Jul;131(7):817-20.
5
Juvenile neutrophilic eccrine hidradenitis: a vasculitis-like plantar dermatosis.青少年嗜中性小汗腺汗管炎:一种类似血管炎的足底皮肤病。
Clin Rheumatol. 2000;19(6):481-3. doi: 10.1007/pl00011181.
6
Idiopathic palmoplantar hidradenitis. Report of three cases and literature review.
Dermatology. 1997;195(4):379-81. doi: 10.1159/000245992.
7
[Palmoplantar neutrophilic eccrine hidradenitis with general extension in a child in remission after acute lymphoblastic leukemia].[急性淋巴细胞白血病缓解期儿童出现泛发性掌跖嗜中性小汗腺汗管炎]
Ann Dermatol Venereol. 2014 Apr;141(4):285-9. doi: 10.1016/j.annder.2014.01.007. Epub 2014 Feb 25.
8
Idiopathic palmoplantar eccrine hidradenitis in children.
Eur J Pediatr. 2001 Mar;160(3):189-91. doi: 10.1007/s004319900193.
9
[Plantar hidradenitis].足底汗腺炎
Acta Med Port. 2001 May-Jun;14(3):371-4.
10
Plantar hidradenitis in children induced by exposure to wet footwear.
Pediatr Emerg Care. 2000 Jun;16(3):182-3. doi: 10.1097/00006565-200006000-00013.

引用本文的文献

1
Pseudomonas-Contaminated Pool Triggering an Episode of Idiopathic Palmoplantar Hidradenitis.假单胞菌污染的泳池引发特发性掌跖汗腺炎发作。
Case Rep Dermatol. 2021 Jul 26;13(2):411-416. doi: 10.1159/000516355. eCollection 2021 May-Aug.