Chen Ping, Li Juan, Liu Ping-Xian, Gou Hui, Yu Ming, Li Lin-Lin, Huang Luwen
Department of Pharmacy, Suining Central Hospital, Suining, China.
Laboratory of Human Diseases and Immunotherapy, West China Hospital, Sichuan University, Chengdu, China.
Front Med (Lausanne). 2025 Aug 11;12:1588977. doi: 10.3389/fmed.2025.1588977. eCollection 2025.
Cerebral nocardiosis caused by represents a rare and diagnostically challenging infectious disease, predominantly affecting immunocompromised patients. This opportunistic infection may also pose life-threatening risks to immunocompetent individuals. The diagnostic process is frequently complicated by the absence of distinctive clinical manifestations and technical limitations inherent to conventional microbiological detection methods, which collectively impede the acquisition of definitive pathogenic evidence, thereby resulting in diagnostic delays. This case report describes a 67-year-old immunocompetent male bricklayer who presented with recurrent febrile episodes during hospitalization and was ultimately diagnosed with purulent meningitis based on clinical history corroborated by cerebrospinal fluid (CSF) analytical findings. Ceftriaxone was initially employed as an anti-infective agent, however, it was ineffective. Consequently, the treatment was escalated to a combination of meropenem and vancomycin, yet the patient's condition did not significantly improve. Concurrently, repeated cultures of the patient's blood and CSF yielded no identifiable pathogens. Notably, three months ago, the patient accidentally sustained a laceration on the left thigh by an unknown object during work. An abscess gradually developed at the site of the laceration, and incision and drainage were carried out at a local hospital. However, the wound did not heal satisfactorily after the surgery, raising concerns about potential rare pathogenic bacterial infections. Ultimately, the pathogen was successfully identified as through metagenomic next-generation sequencing (mNGS). Following this diagnosis, the patient's condition was rapidly controlled after initiating treatment with the targeted drug combination of sulfamethoxazole, meropenem, and amikacin. Given the high misdiagnosis rate and poor sensitivity of cultures for in cases of intracranial infections, this case underscores the critical role of mNGS in the diagnosis and selection of effective antibiotics for treating intracranial infections.
由[未提及具体病原体名称]引起的脑诺卡菌病是一种罕见且诊断具有挑战性的传染病,主要影响免疫功能低下的患者。这种机会性感染对免疫功能正常的个体也可能构成危及生命的风险。诊断过程常常因缺乏独特的临床表现以及传统微生物检测方法固有的技术局限性而变得复杂,这些因素共同阻碍了获取明确的致病证据,从而导致诊断延迟。本病例报告描述了一名67岁免疫功能正常的男性砖匠,他在住院期间出现反复发热,最终根据脑脊液(CSF)分析结果证实的临床病史被诊断为化脓性脑膜炎。最初使用头孢曲松作为抗感染药物,但无效。因此,治疗升级为美罗培南和万古霉素联合使用,但患者病情并未明显改善。同时,对患者的血液和脑脊液进行多次培养均未发现可识别的病原体。值得注意的是,三个月前,患者在工作期间左大腿被不明物体意外划伤。伤口处逐渐形成脓肿,并在当地医院进行了切开引流。然而,手术后伤口愈合不佳,引发了对潜在罕见病原菌感染的担忧。最终,通过宏基因组下一代测序(mNGS)成功鉴定出病原体为[未提及具体病原体名称]。确诊后,在开始使用磺胺甲恶唑、美罗培南和阿米卡星的靶向药物联合治疗后,患者病情迅速得到控制。鉴于颅内感染病例中[未提及具体病原体名称]培养的误诊率高且敏感性差,本病例强调了mNGS在诊断和选择治疗[未提及具体病原体名称]颅内感染的有效抗生素方面的关键作用。