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表现为急性化脓性腮腺炎的迟发性B族链球菌病

Late onset group B streptococcus disease manifesting as acute suppurative parotitis.

作者信息

Ujita Nagisa, Kawasaki Yu, Matsubara Kousaku, Kim Kaya, Naito Akiyoshi, Hori Masayuki, Isome Kenichi, Iwata Aya, Yamaguchi Yoshimichi, Chang Bin

机构信息

Department of Pediatrics, Kobe City Nishi-Kobe Medical Center, Kobe, Japan.

Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

IDCases. 2020 May 11;21:e00799. doi: 10.1016/j.idcr.2020.e00799. eCollection 2020.

DOI:10.1016/j.idcr.2020.e00799
PMID:32461904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7242865/
Abstract

Few patients with acute suppurative parotitis (ASP) due to group B streptococcus (GBS) have been documented. Limited data on clinical and microbiological features and infectious route are available. We present a 21-day-old boy with invasive GBS disease manifesting as ASP. The patient was admitted because of irritability, fever, and erythematous swelling over the right parotid area. No purulent material exuded from the Stensen's duct. Ultrasonography and computed tomography of the neck showed findings indicative of ASP. On the day after admission, blood culture yielded GBS. The isolate was determined as GBS serotype Ia and sequence type-23, and the patient was successfully treated with intravenous ampicillin for 10 days. A review of the literature revealed 11 GBS ASP infants including ours with age at onset between 13 days and 12 weeks. All infants had bacteremia while pus from the Stensen's duct was detected in only one case. This finding remarkably contrasts with ASP caused by pathogens other than GBS, where the infection usually spreads via a retrograde route from Stensen's duct. The present case and literature review indicate GBS ASP primarily arises from bloodstream infection, and that ASP should be included in an infectious focus as late onset GBS disease.

摘要

由B组链球菌(GBS)引起的急性化脓性腮腺炎(ASP)患者鲜有文献记载。关于临床和微生物学特征以及感染途径的数据有限。我们报告一名21日龄男婴,患有侵袭性GBS疾病,表现为ASP。该患者因烦躁、发热及右腮腺区红肿入院。腮腺导管未见脓性分泌物渗出。颈部超声和计算机断层扫描结果提示为ASP。入院次日,血培养检出GBS。分离株鉴定为GBS血清型Ia和序列型-23,患者接受静脉注射氨苄西林治疗10天,治疗成功。文献回顾发现11例GBS-ASP婴儿,包括我们的病例,发病年龄在13天至12周之间。所有婴儿均有菌血症,仅1例在腮腺导管脓性分泌物中检测到病原体。这一发现与非GBS病原体引起的ASP显著不同,后者感染通常通过腮腺导管逆行传播。本病例及文献回顾表明,GBS-ASP主要源于血流感染,ASP应作为晚发性GBS疾病的感染灶之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/613b/7242865/e1a58d742e03/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/613b/7242865/e1a58d742e03/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/613b/7242865/e1a58d742e03/gr1.jpg

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