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由乔治西诺卡菌引起的胫骨干骨髓炎罕见病例。

Rare case of osteomyelitis of tibial shaft caused by Nocardia cyriacigeorgica.

作者信息

Raszka D, Popelka S, Heřt J, Jahoda D, Landor I, Vavřík P

机构信息

Department of Orthopaedics, First Faculty of Medicine, Charles University in Prague and Motol University Hospital, V Úvalu 84, 150 06, Prague 5, Czech Republic.

出版信息

Folia Microbiol (Praha). 2018 Jul;63(4):525-532. doi: 10.1007/s12223-018-0589-0. Epub 2018 Mar 5.

Abstract

Nocardiosis is a rare infection caused by the aerobic actinomycete of the Nocardia genus. In most cases, nocardiosis manifests as a lung infection or a bone lesion. Due to the nonspecific and mild clinical manifestations of nocardiosis, the establishment of definite diagnosis can be difficult. When antibiotic therapy is incorrectly targeted, only the symptoms of the disease are suppressed. The mainstay in the treatment of Nocardia osteomyelitis has so far been the combined surgical debridement with long-term, initially intravenous, antibiotic administration. We present the successful conservative treatment of a nocardiosis osteomyelitis of the tibia caused by the Nocardia cyriacigeorgica species in an 81-year-old female patient that manifested itself as a secondary affection on top of a primary nocardiosis infection of the lung. From microbiological examination, N. cyriacigeorgica was discovered; the identification was made using matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS) with an identification score of 1.9. The sensitivity was evaluated using E test. Sensitivity to trimethoprim/sulfamethoxazole, amikacin, imipenem, and linezolid was demonstrated. The bacteria were shown to be resistant to ciprofloxacin. For treatment, trimethoprim/sulfamethoxazole was used due to the value of minimum inhibitory concentration, which was 0.25 mg/L. The initial dose of 960 mg of trimethoprim/sulfamethoxazole every 8 h was reduced to 960 mg every 12 h after 3 months. The total duration of treatment was 7.5 months. Under the established treatment, the bone and lung lesions healed. Nocardiosis of the long bone is considered a rare disease and its precise diagnosis has not yet been standardized. We used the MALDI-TOF MS method for the identification of the causal organism which is a fast and reliable method according to current world literature even when compared with the rRNA genetic sequencing reference method. Our case study presents a rare case of osteomyelitis of tibial shaft caused by N. cyriacigeorgica and its successful conservative treatment.

摘要

诺卡菌病是由诺卡菌属需氧放线菌引起的一种罕见感染。在大多数情况下,诺卡菌病表现为肺部感染或骨病变。由于诺卡菌病的临床表现不具特异性且较为轻微,明确诊断可能会有困难。当抗生素治疗靶向错误时,只会抑制疾病症状。迄今为止,治疗诺卡菌性骨髓炎的主要方法是联合手术清创并长期(最初为静脉注射)使用抗生素。我们报告了一例81岁女性患者由乔治西里亚克诺卡菌引起的胫骨诺卡菌病骨髓炎的成功保守治疗病例,该病例表现为在肺部原发性诺卡菌病感染基础上的继发性病变。通过微生物学检查发现了乔治西里亚克诺卡菌;使用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)进行鉴定,鉴定分数为1.9。使用E试验评估敏感性。结果显示对甲氧苄啶/磺胺甲恶唑、阿米卡星、亚胺培南和利奈唑胺敏感。该细菌对环丙沙星耐药。由于最低抑菌浓度为0.25mg/L,因此使用甲氧苄啶/磺胺甲恶唑进行治疗。最初每8小时服用960mg甲氧苄啶/磺胺甲恶唑,3个月后减至每12小时960mg。治疗总时长为7.5个月。在既定治疗方案下,骨和肺部病变均愈合。长骨诺卡菌病被认为是一种罕见疾病,其精确诊断尚未标准化。我们使用MALDI-TOF MS方法鉴定病原体,根据当前世界文献,即使与rRNA基因测序参考方法相比,这也是一种快速可靠的方法。我们的病例研究展示了一例由乔治西里亚克诺卡菌引起的胫骨干骨髓炎罕见病例及其成功的保守治疗。

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