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儿科放线菌病:16 年单机构回顾性病例研究。

Paediatric actinomycosis: A 16-year, single-institution retrospective review of cases.

机构信息

Department of Pediatric Medicine, KK Women's and Children's Hospital, Singapore.

Infectious Disease Service, Department of Pediatric Medicine, KK Women's and Children's Hospital, Singapore.

出版信息

J Paediatr Child Health. 2023 Jun;59(6):833-839. doi: 10.1111/jpc.16400. Epub 2023 Apr 5.

Abstract

AIM

Actinomycosis is a rare subacute to chronic granulomatous infection which can mimic other infectious or malignant diseases. This study examined the epidemiology and treatment outcome of actinomycosis in children.

METHODS

A retrospective study on children admitted for actinomycosis in a tertiary paediatric hospital in Singapore, from January 2004 to December 2020. Clinical profile, therapeutic interventions and outcomes were examined.

RESULTS

A total of 10 patients were identified; 7 were female. The median age at first presentation was 9.8 years (range 4.7-15.7). The most common presenting symptom was fever (n = 6, 60%), followed by facial or neck swelling (n = 3, 30%) and ear pain (n = 3, 30%). Actinomycosis occurred predominantly in the orocervicofacial region (n = 6, 60%). Four patients (40%) had preceding dental infections in the form of dental caries or gingivitis. One patient had poorly controlled insulin-dependent diabetes mellitus. Actinomycosis was confirmed via culture in four patients, histopathology in four patients and both methods in two patients. All except one patient (n = 9, 90%) underwent surgical procedures. All patients received ampicillin or amoxicillin/clavulanate or other beta-lactams, for a median duration of 6.5 months (range 1.5-14). Complications included osteomyelitis (n = 4, 40%), mastoiditis (n = 2, 20%), brain abscess (n = 1, 10%) and recurrent neck abscess (n = 1, 10%). There was no mortality and all patients achieved complete resolution.

CONCLUSIONS

Paediatric actinomycosis was rare in our 16-year review, but had a high complication rate. It can occur in immunocompetent patients, and dental infection was the predominant risk factor identified. Prognosis was excellent after surgical intervention and appropriate antimicrobial therapy.

摘要

目的

放线菌病是一种罕见的亚急性至慢性肉芽肿性感染,可模仿其他传染性或恶性疾病。本研究探讨了儿童放线菌病的流行病学和治疗结果。

方法

对 2004 年 1 月至 2020 年 12 月在新加坡一家三级儿科医院就诊的放线菌病患儿进行回顾性研究。检查了临床特征、治疗干预措施和结果。

结果

共确定了 10 名患者;7 名女性。首次就诊时的中位年龄为 9.8 岁(范围为 4.7-15.7)。最常见的首发症状是发热(n=6,60%),其次是面部或颈部肿胀(n=3,30%)和耳痛(n=3,30%)。放线菌病主要发生在口咽面颈部(n=6,60%)。4 名患者(40%)有龋齿或牙龈炎等先前的牙科感染。1 名患者患有未控制的胰岛素依赖型糖尿病。4 名患者(40%)通过培养、4 名患者通过组织病理学和 2 名患者通过两种方法确认放线菌病。除 1 名患者(n=9,90%)外,所有患者均接受手术治疗。所有患者均接受氨苄西林或阿莫西林/克拉维酸或其他β-内酰胺类药物治疗,中位疗程为 6.5 个月(范围 1.5-14)。并发症包括骨髓炎(n=4,40%)、乳突炎(n=2,20%)、脑脓肿(n=1,10%)和颈部脓肿复发(n=1,10%)。无死亡病例,所有患者均完全缓解。

结论

在我们 16 年的回顾中,儿科放线菌病很少见,但并发症发生率很高。它可发生于免疫功能正常的患者,且牙科感染是确定的主要危险因素。经手术干预和适当的抗菌治疗后,预后良好。

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