Tularemia in Pediatric Patients: A Case Series and Review of the Literature.

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Remadji Fiona Kossadoum, Audrey Baron, Marie Parizot, Maya Husain, Nora Poey, Max Maurin, Yvan Caspar, Marion Caseris, Philippe Bidet, Stephane Bonacorsi
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Abstract

Background: Unfamiliar to pediatricians, tularemia can lead to delays in diagnosis and hinder appropriate treatment, as its clinical presentation often shares similarities with other more prevalent causes of lymphadenopathy diseases in children. We conducted a comprehensive literature review to offer contemporary insights into the clinical manifestations and treatment strategies for tularemia infection in children.

Methods: Three cases of glandular tularemia were diagnosed in the Pediatric Robert Debré Hospital (Paris) between October 2020 and February 2022. In addition, we conducted a literature search using PubMed in December 2023 of cases of tularemia in children published in English.

Results: The 94 cases of the literature review highlight the large age range (from 6 weeks to 17 years) and multiple sources of infection, including diverse zoonotic transmission (86.7%) and contact with contaminated water (13.3%). Fever was a consistent symptom. Ulceroglandular (46.7%), glandular (17%) and oropharyngeal forms (18.1%) predominated. The most frequently used diagnostic method was serology (60.6%). The median time to diagnosis for tularemia was 23.5 days. Hospitalization was required in 63.2% of cases, with a median duration of 4 days. Targeted treatment was based on aminoglycosides (37.6%), fluoroquinolones (30.6%) or tetracyclines (12.9%), in accordance with WHO recommendations, with a mainly favorable outcome, although several cases of meningitis were observed.

Conclusion: Pediatricians should be aware of the etiology of this febrile lymphadenopathy, notably when experiencing beta-lactam treatment failure, even in young infants, which could help reduce the extra costs associated with inappropriate antibiotic use and hospitalization.

小儿患者中的图拉里病毒:病例系列和文献综述。
背景:由于土拉菌病的临床表现往往与其他更常见的儿童淋巴腺病病因相似,儿科医生对其并不熟悉,因此可能导致诊断延误并妨碍适当的治疗。我们进行了一次全面的文献综述,以提供有关儿童感染土拉菌病的临床表现和治疗策略的最新见解:2020年10月至2022年2月期间,罗伯特-德布雷儿科医院(巴黎)确诊了3例腺土拉菌病病例。此外,我们在 2023 年 12 月使用 PubMed 对英文发表的儿童土拉菌病病例进行了文献检索:文献综述中的94个病例强调了较大的年龄范围(从6周到17岁)和多种感染源,包括多种人畜共患病传播(86.7%)和接触污染水源(13.3%)。发热是一种常见症状。溃疡型(46.7%)、腺型(17%)和口咽型(18.1%)占多数。最常用的诊断方法是血清学(60.6%)。确诊土拉菌病的中位时间为 23.5 天。63.2%的病例需要住院治疗,中位住院时间为 4 天。根据世界卫生组织的建议,采用氨基糖苷类药物(37.6%)、氟喹诺酮类药物(30.6%)或四环素类药物(12.9%)进行针对性治疗,结果主要良好,但也发现了几例脑膜炎病例:儿科医生应了解这种发热性淋巴结病的病因,尤其是在β-内酰胺类药物治疗失败时,即使是年幼的婴儿也应如此,这有助于减少与抗生素使用不当和住院治疗相关的额外费用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
2.80%
发文量
566
审稿时长
2-4 weeks
期刊介绍: ​​The Pediatric Infectious Disease Journal® (PIDJ) is a complete, up-to-the-minute resource on infectious diseases in children. Through a mix of original studies, informative review articles, and unique case reports, PIDJ delivers the latest insights on combating disease in children — from state-of-the-art diagnostic techniques to the most effective drug therapies and other treatment protocols. It is a resource that can improve patient care and stimulate your personal research.
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