• 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

B 型链球菌蜂窝织炎和坏死性筋膜炎在婴儿中的表现:系统综述。

Group B Streptococcal Cellulitis and Necrotizing Fasciitis in Infants: A Systematic Review.

机构信息

From the Schulich School of Medicine and Dentistry.

Department of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, Canada.

出版信息

Pediatr Infect Dis J. 2018 Sep;37(9):e241-e245. doi: 10.1097/INF.0000000000001931.

DOI:10.1097/INF.0000000000001931
PMID:29424798
Abstract

BACKGROUND

There is no consensus regarding approaches to infantile group B streptococcal (GBS) head and neck cellulitis and necrotizing fasciitis. We present a case of GBS necrotizing cellulitis and summarize the literature regarding the presentation and management of infantile head and neck GBS cellulitis and necrotizing fasciitis.

METHODS

The literature was searched using PubMed, Web of Science, EMBASE and Medline (inception to April 2017) by 2 independent review authors. Inclusion criteria encompassed case reports or case series of infants less than 12 months of age with GBS cellulitis of the head and neck or with GBS necrotizing fasciitis without restriction to the head and neck. Data were extracted using tables developed a priori by 2 independent review authors, and discrepancies were resolved by consensus.

RESULTS

An infant presenting at 33 days of age with GBS facial necrotizing fasciitis was successfully treated conservatively with antibiotics. Our literature search identified 40 infants with GBS head and neck cellulitis. Late-onset (98%), male gender (65%) and prematurity (58%) predominated. Penicillin is the main therapy used (97%). The 12 identified cases of necrotizing fasciitis were associated with polymicrobial etiology (36%) and broad-spectrum antibiotic use. Seventy-five percent required debridement, including 4 of 5 (80%) cases involving the head and neck.

CONCLUSIONS

Skin and soft tissue involvement is an uncommon manifestation of late-onset GBS infection which requires antibiotic therapy and possibly surgical debridement cases with necrotizing fasciitis.

摘要

背景

对于婴儿 B 群链球菌(GBS)头颈部蜂窝织炎和坏死性筋膜炎的治疗方法尚无共识。我们报告了一例 GBS 坏死性蜂窝织炎病例,并总结了有关婴儿头颈部 GBS 蜂窝织炎和坏死性筋膜炎表现和处理的文献。

方法

两名独立的综述作者使用 PubMed、Web of Science、EMBASE 和 Medline(从创建到 2017 年 4 月)检索文献。纳入标准包括婴儿小于 12 个月,有 GBS 头颈部蜂窝织炎或 GBS 坏死性筋膜炎,不局限于头颈部。使用由两名独立综述作者预先制定的表格提取数据,如有分歧则通过协商解决。

结果

一名 33 天大的婴儿患有 GBS 面部坏死性筋膜炎,经抗生素保守治疗成功。我们的文献检索共确定了 40 例 GBS 头颈部蜂窝织炎患儿。晚发型(98%)、男性(65%)和早产(58%)为主。青霉素是主要治疗药物(97%)。12 例明确的坏死性筋膜炎与多微生物病因(36%)和广谱抗生素使用有关。75%的患儿需要清创,其中 4 例(80%)涉及头颈部。

结论

皮肤和软组织受累是晚发型 GBS 感染的罕见表现,需要抗生素治疗,可能需要手术清创,坏死性筋膜炎病例则需要清创。

相似文献

1
Group B Streptococcal Cellulitis and Necrotizing Fasciitis in Infants: A Systematic Review.B 型链球菌蜂窝织炎和坏死性筋膜炎在婴儿中的表现:系统综述。
Pediatr Infect Dis J. 2018 Sep;37(9):e241-e245. doi: 10.1097/INF.0000000000001931.
2
Necrotizing fasciitis: a rare manifestation of late-onset neonatal group B streptococcal infection.坏死性筋膜炎:晚发性新生儿B族链球菌感染的一种罕见表现。
J Med Assoc Thai. 2014 Jun;97(6):669-72.
3
Case report and literature review of late-onset group B streptococcal disease manifesting as necrotizing fasciitis in preterm infants: is this a new syndrome?以坏死性筋膜炎为表现的早产儿晚发性B族链球菌病病例报告及文献综述:这是一种新综合征吗?
Clin Infect Dis. 2003 Nov 1;37(9):e132-5. doi: 10.1086/378892. Epub 2003 Oct 3.
4
An aggressive group a streptococcal cellulitis of the hand and forearm requiring surgical debridement.一例侵袭性手部和前臂A组链球菌蜂窝织炎,需行手术清创。
Orthopedics. 2011 Jan 3;34(1):57. doi: 10.3928/01477447-20101123-26.
5
Three fatal cases of invasive serotype VI group B streptococcal infection.3例侵袭性B族链球菌血清型VI感染致死病例。
J Infect. 2006 Sep;53(3):e139-42. doi: 10.1016/j.jinf.2005.11.023. Epub 2006 Jan 3.
6
Facial submandibular cellulitis associated with late-onset group B streptococcal infection.与迟发性B族链球菌感染相关的面部颌下蜂窝织炎
Adv Neonatal Care. 2004 Feb;4(1):20-5. doi: 10.1016/j.adnc.2003.11.010.
7
A Rare Case of Monomicrobial Necrotizing Fasciitis Associated With an Initial Acute Compartment Syndrome.单一细菌坏死性筋膜炎伴初始急性间隔综合征一例罕见病例报告。
J Foot Ankle Surg. 2022 Jan-Feb;61(1):195-198. doi: 10.1053/j.jfas.2021.08.005. Epub 2021 Aug 18.
8
Periorbital necrotizing fasciitis: clinical perspectives on nine cases.眶周坏死性筋膜炎:9 例临床观察。
Eur J Clin Microbiol Infect Dis. 2024 Oct;43(10):2053-2059. doi: 10.1007/s10096-024-04908-6. Epub 2024 Jul 31.
9
A case of facial cellulitis caused by group B streptococcus in an extremely low birthweight infant.一例极低出生体重儿由 B 群链球菌引起的面部蜂窝织炎。
J Infect Chemother. 2021 Sep;27(9):1369-1372. doi: 10.1016/j.jiac.2021.04.021. Epub 2021 May 11.
10
Retiform Purpura as a Sign of Necrotizing Cellulitis in an Immunocompetent Boy.网状青斑:免疫功能正常男孩坏死性蜂窝织炎的征象。
Pediatr Emerg Care. 2020 Nov;36(11):e646-e648. doi: 10.1097/PEC.0000000000002251.

引用本文的文献

1
Faciocervical Group B Necrotising Fasciitis: a Multidisciplinary Approach Management.面颈部B组坏死性筋膜炎:多学科综合管理方法
BMJ Case Rep. 2023 Dec 7;16(12):e255874. doi: 10.1136/bcr-2023-255874.
2
Group B streptococcus sepsis in an infant presented with cellulitis of soft tissue of neck.婴儿因 B 组链球菌败血症引起颈部软组织蜂窝织炎。
BMJ Case Rep. 2021 Aug 11;14(8):e241683. doi: 10.1136/bcr-2021-241683.
3
Necrotizing fasciitis in a 5-week-old infant: An unusual presentation.一名5周大婴儿的坏死性筋膜炎:一种不寻常的表现。
SAGE Open Med Case Rep. 2021 Jul 29;9:2050313X211037121. doi: 10.1177/2050313X211037121. eCollection 2021.