From the Schulich School of Medicine and Dentistry.
Department of Otolaryngology-Head and Neck Surgery, Western University, London, Ontario, Canada.
Pediatr Infect Dis J. 2018 Sep;37(9):e241-e245. doi: 10.1097/INF.0000000000001931.
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.
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.
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.
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.
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。
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。
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。
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。