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一名3岁儿童疑似巴尔通体相关性脊椎椎间盘炎:病例报告及文献综述

Presumed Bartonella-Associated Spondylodiscitis in a 3-Year-Old Child: A Case Report and Review of the Literature.

作者信息

El Assaad Hadi, Schumann Eckehard, Klemann Christian, Dietze-Jergus Nadine, Heyde Christoph-Eckhard, Pieroh Philipp

机构信息

Department of Orthopedics, Trauma and Plastic Surgery, University of Leipzig, 04103 Leipzig, Germany.

Department of Pediatric Immunology, Rheumatology and Infectiology, Hospital for Children and Adolescents, University of Leipzig, 04103 Leipzig, Germany.

出版信息

Children (Basel). 2025 May 16;12(5):649. doi: 10.3390/children12050649.

Abstract

With an incidence of 0.3 per 100,000, spondylodiscitis is a rare condition in children. It is typically bacterial in origin and most commonly caused by . Bone involvement in cat-scratch disease (CSD) due to is exceedingly rare, occurring in only 0.17-0.27% of cases. We present the case of a 3-year-old boy with a two-week history of intermittent back pain and a recent onset fever. Initial laboratory findings were unremarkable, and MRI revealed spondylodiscitis at L3/4 without abscess formation. Empirical antibiotic treatment with ampicillin/sulbactam showed no clinical response. Serologic testing revealed a positive IgM (IgG negative), leading to a change in antibiotic treatment to azithromycin and rifampicin for three weeks, resulting in rapid clinical improvement. Follow-up at nine weeks showed marked clinical and radiologic improvement. Although IgM subsequently turned negative without IgG seroconversion-a pattern previously described in infections-this does not exclude the diagnosis. Biopsy or tissue PCR was not performed due to the mild clinical course. A review of the literature identified 28 pediatric cases of spondylodiscitis, with significant variation in diagnostic and treatment approaches. This case underscores the importance of considering in the differential diagnosis of pediatric vertebral osteomyelitis.

摘要

脊椎椎间盘炎在儿童中发病率为每10万人0.3例,是一种罕见疾病。其通常起源于细菌,最常见的病因是 。由 引起的猫抓病(CSD)累及骨骼极为罕见,仅在0.17 - 0.27%的病例中出现。我们报告一例3岁男孩病例,其有两周间歇性背痛病史且近期发热。初始实验室检查结果无异常,MRI显示L3/4椎体椎间盘炎,无脓肿形成。氨苄西林/舒巴坦经验性抗生素治疗无临床反应。血清学检测显示 IgM阳性(IgG阴性),抗生素治疗改为阿奇霉素和利福平,持续三周,临床症状迅速改善。九周后随访显示临床和影像学有显著改善。尽管IgM随后转为阴性且未出现IgG血清学转换——这是先前在 感染中描述过的模式——但这并不排除诊断。由于临床病程较轻,未进行活检或组织PCR检测。文献回顾发现28例儿童 椎体椎间盘炎病例,诊断和治疗方法差异很大。该病例强调了在儿童椎体骨髓炎鉴别诊断中考虑 的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e498/12110131/1ddeb3638e06/children-12-00649-g001.jpg

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