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免疫功能低下儿童和新生儿骨髓炎病例系列研究。

Osteomyelitis in Immunocompromised children and neonates, a case series.

机构信息

Singapore General Hospital, Singapore, Singapore.

Department of Orthopedic Surgery, KK Women's and Children's Hospital, Singapore, Singapore.

出版信息

BMC Pediatr. 2021 Dec 11;21(1):568. doi: 10.1186/s12887-021-03031-1.

Abstract

BACKGROUND

Osteomyelitis in immunocompromised children can present differently from immunocompetent children and can cause devastating sequelae if treated inadequately. We aim to review the aetiology, clinical profile, treatment and outcomes of immunocompromised children with osteomyelitis.

METHODS

Retrospective review of all immunocompromised children aged < 16 years and neonates admitted with osteomyelitis in our hospital between January 2000 and January 2017, and referred to the Paediatric Infectious Disease Service.

RESULTS

Fourteen patients were identified. There were 10 boys (71%), and the median age at admission was 70.5 months (inter-quartile range: 12.3-135.0 months). Causal organisms included, two were Staphylococcus aureus, two were Mycobacterium bovis (BCG), and one each was Mycobacterium tuberculosis, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, Burkholderia pseudomallei and Rhizopus sp. One patient had both Clostridium tertium and Clostridium difficile isolated. Treatment involved appropriate antimicrobials for a duration ranging from 6 weeks to 1 year, and surgery in 11 patients (79%). Wherever possible, the patients received treatment for their underlying immunodeficiency. For outcomes, only three patients (21%) recovered completely. Five patients (36%) had poor bone growth, one patient had recurrent discharge from the bone and one patient had palliative care for underlying osteosarcoma.

CONCLUSIONS

Although uncommon, osteomyelitis in immunocompromised children and neonates can be caused by unusual pathogens, and can occur with devastating effects. Treatment involves prolonged administration of antibiotics and surgery. Immune recovery also seems to be an important factor in bone healing.

摘要

背景

免疫功能低下儿童的骨髓炎与免疫功能正常儿童的骨髓炎表现不同,如果治疗不当,可能会导致严重的后遗症。我们旨在回顾免疫功能低下儿童骨髓炎的病因、临床特征、治疗和结局。

方法

回顾性分析 2000 年 1 月至 2017 年 1 月期间我院收治的所有年龄<16 岁的免疫功能低下儿童和新生儿骨髓炎患者,并将其转至儿科传染病科。

结果

共确定了 14 名患者。其中男性 10 例(71%),入院时的中位年龄为 70.5 个月(四分位距:12.3-135.0 个月)。病原体包括 2 株金黄色葡萄球菌、2 株牛型分枝杆菌(BCG)、1 株结核分枝杆菌、1 株铜绿假单胞菌、1 株嗜麦芽寡养单胞菌、1 株鼻疽伯克霍尔德菌和 1 株根霉。1 例患者同时分离出梭状芽孢杆菌和艰难梭菌。治疗包括使用适当的抗生素治疗 6 周至 1 年,并对 11 例患者(79%)进行手术。只要有可能,患者均接受针对潜在免疫缺陷的治疗。就结局而言,仅有 3 例患者(21%)完全康复。5 例患者(36%)存在骨骼生长不良,1 例患者骨骼持续有分泌物排出,1 例患者因潜在骨肉瘤而接受姑息治疗。

结论

尽管罕见,但免疫功能低下儿童和新生儿的骨髓炎可由不常见的病原体引起,并可能产生严重的后果。治疗需要长期使用抗生素和手术。免疫恢复似乎也是骨愈合的一个重要因素。

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本文引用的文献

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Acute Hematogenous Osteomyelitis in Children.儿童急性血源性骨髓炎
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