潜伏17年后胫骨耐甲氧西林金黄色葡萄球菌骨髓炎的再激活:1例报告和文献复习

C. Fryer
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引用次数: 0

摘要

简介:金黄色葡萄球菌是骨髓炎最常见的原因,具有显著的发病率和死亡率。甲氧西林敏感金黄色葡萄球菌骨髓炎在原发性发作数年后再激活是一种众所周知的现象。然而,很少有病例报告记录休眠耐甲氧西林金黄色葡萄球菌骨髓炎复发数年后。我们的病例报告显示,潜伏的耐甲氧西林金黄色葡萄球菌胫骨骨髓炎在17年后重新激活,代表了从耐甲氧西林金黄色葡萄球菌首次发作以来最长的复发间隔之一,以及所涉及的诊断和治疗挑战。病例报告:一名55岁男性报告2004年发生Gustilo & Anderson 1级开放性左胫骨平台骨折,采用伤口清创和Taylor空间框架治疗。最初的治疗是清创和初步缝合伤口,并应用泰勒空间框架(TSF)作为骨折的最终治疗。应用框架一个月后,患者报告他遭受针部感染。这被发现是感染骨髓炎MRSA。创面行手术清创,3个月骨折愈合后取出外支架,髓内扩孔冲洗。不需要进一步的软组织覆盖。患者接受延长疗程的静脉万古霉素治疗,随后口服克林霉素。自此发作以来,患者无症状,拒绝进一步住院治疗,患者完全恢复功能,没有任何限制。患者未报告任何复发性伤口、分泌物、鼻窦或疼痛。十七年后,在膝盖受到闭合性打击后,患者出现膝盖疼痛的发热症状。他被发现患有耐甲氧西林金黄色葡萄球菌胫骨骨髓炎,主要集中在胫骨近内侧皮质。治疗方法是有针对性的手术清创,抗生素指甲和长期抗生素。患者6个月后仍无症状,感染明显消退。结论:本病例是罕见的耐甲氧西林金黄色葡萄球菌复发间隔最长的病例之一。耐甲氧西林金黄色葡萄球菌骨髓炎患者应接受适当的治疗,并与骨科医生和传染病医生进行随访,以监测疾病进展并确保感染得到解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactivation of Dormant Tibial Methicillin- Resistant Staphylococcus aureus Osteomyelitis after 17 Years: A Case Report and Literature Review
Introduction: Staphylococcus aureus is the most common cause of osteomyelitis with significant morbidity and mortality outcomes. Methicillin-susceptible Staphylococcus aureus osteomyelitis reactivation years after the primary episode are a well-known phenomenon. However, there are few case reports documenting dormant Methicillin-Resistant Staphylococcus aureus osteomyelitis recurrence years later. Our case report of dormant Methicillin-Resistant Staphylococcus aureus tibial osteomyelitis reactivation after 17-years, represents one of the longest documented recurrence intervals from initial bout of Methicillin-Resistant Staphylococcus aureus , as well as, the diagnostic and therapeutic challenges involved. Case report: A 55-year-old male reports suffering a Gustilo & Anderson grade 1 open left tibial plafond fracture in 2004 that was managed with wound debridement and Taylor Spatial Frame. Initial management was with debridement and primary closure of the wound and application of a Taylor spatial frame (TSF) as definitive management of the fracture. One month following application of the frame, the patient reports he suffered a pin site infection. This was found to be infected osteomyelitis MRSA. The wound underwent surgical debridement and once the fracture was consolidated enough at three months, removal of external frame and intramedullary reaming and irrigation was performed. No further soft tissue coverage was required. The patient was treated with a prolonged course of intravenous vancomycin, followed by oral clindamycin. Since this episode, the patient has been asymptomatic and denied any further hospitalisations and the patient returned to full function without any limitations. The patient does not report any recurrent wounds, discharge, sinus or pain. Seventeen years later, after a closed blow to the knee, the patient present febrile with knee pain. He was found to have Methicillin-Resistant Staphylococcus aureus tibial osteomyelitis, most concentrated in the proximal medial tibial cortex. This was treated with targeted surgical debridement, an antibiotic nail and prolonged antibiotics. The patient has remained asymptomatic with apparent resolution of infection 6-months post. Conclusion: Our case report represents one of rare and longest document recurrence intervals of Methicillin-Resistant Staphylococcus aureus . Patients with Methicillin-Resistant Staphylococcus aureus osteomyelitis should have appropriate treatment and follow-up with orthopaedic surgeons and infectious disease physicians to monitor disease progression and to ensure resolution of the infection.
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