Fusobacterium necrophorum

坏死梭杆菌
  • 文章类型: Journal Article
    背景:军团菌肺炎是非典型肺炎中最严重的类型之一,损害多器官系统,对生命构成威胁.由于培养细菌的困难以及免疫测定灵敏度和特异性的限制,军团菌肺炎的诊断具有挑战性。
    方法:本文报道一例罕见的由嗜肺军团菌和坏死梭菌联合感染引起的脓毒症,导致呼吸衰竭,急性肾损伤,急性肝损伤,心肌损伤,和电解质紊乱。此外,我们系统回顾了军团菌联合感染患者的文献,分析他们的临床特征,实验室结果和诊断。
    结论:对于需要延长潜伏期且对常规培养方法不太敏感的病原体,宏基因组下一代测序(mNGS)可以作为病原体筛查的有力补充,在复杂传染病的辅助诊断中起着重要作用。
    BACKGROUND: Legionella pneumonia is one of the most severe types of atypical pneumonia, impairing multiple organ systems, posing a threat to life. Diagnosing Legionella pneumonia is challenging due to difficulties in culturing the bacteria and limitations in immunoassay sensitivity and specificity.
    METHODS: This paper reports a rare case of sepsis caused by combined infection with Legionella pneumophila and Fusobacterium necrophorum, leading to respiratory failure, acute kidney injury, acute liver injury, myocardial damage, and electrolyte disorders. In addition, we systematically reviewed literature on patients with combined Legionella infections, analyzing their clinical features, laboratory results and diagnosis.
    CONCLUSIONS: For pathogens that require prolonged incubation periods and are less sensitive to conventional culturing methods, metagenomic next-generation sequencing (mNGS) can be a powerful supplement to pathogen screening and plays a significant role in the auxiliary diagnosis of complex infectious diseases.
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  • 文章类型: Case Reports
    我们描述了一例24岁的男子,该男子患有由坏死梭菌亚种引起的多器官衰竭。F1260.这是第一个描述的Lemierre综合征的病例,该综合征由于F.死角亚种而导致多器官功能衰竭。中国成年人的F1260。我们的研究强调,仅基于颈内静脉血栓性静脉炎的典型表现,可能存在误诊的风险。转移性病变,和从血液培养物或正常无菌部位分离的坏死F.临床医生应该认识到宏基因组下一代测序在促进严重感染的早期病原体检测方面的潜在效用。从而使抗生素的及时和适当的管理,以降低死亡率和改善预后。
    We described a case of a 24-year-old man with multiple organ failure caused by Fusobacterium necrophorum subsp. funduliforme F1260. This is the first described case of Lemierre\'s syndrome with multiple organ failure due to F. necrophorum subsp. funduliforme F1260 in an adult in China. Our study highlights that there may be a risk of misdiagnosis based solely on typical manifestations of internal jugular vein thrombophlebitis, metastatic lesions, and F. necrophorum isolated from blood cultures or normally sterile sites. Clinicians should be cognizant of the potential utility of metagenomic next-generation sequencing in facilitating early pathogen detection in severe infections, thus enabling timely and appropriate administration of antibiotics to reduce mortality rates and improve prognosis.
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  • 文章类型: Case Reports
    Lemierre综合征(LS)是一种罕见且危及生命的疾病,主要由坏死梭杆菌引起。目前,目前尚无针对LS管理的标准化临床指南.这里,我们描述了一个40岁男性发烧的案例,生产性咳嗽,呼吸困难但没有喉咙痛.诊断性放射学检查显示多个肺空洞结节和颈内静脉阻塞。肺泡灌洗液的宏基因组下一代测序(mNGS)鉴定了坏死梭杆菌,从而确认LS的诊断。有趣的是,尽管接受了适当的抗生素,患者仍表现出延迟的临床反应.在将替加环素整合到治疗中以解决潜在的共同感染细菌后,我们观察到他的临床症状明显改善。出院后12周的后续随访显示症状完全缓解,胸部CT扫描显示肺部病变明显消退。
    Lemierre syndrome (LS) is a rare and life-threatening condition predominantly caused by Fusobacterium necrophorum. Currently, there are no standardized clinical guidelines for LS management. Here, we describe the case of a 40-year-old male with fever, productive cough, and dyspnea but no sore throat. Diagnostic radiological examinations revealed multiple pulmonary cavitary nodules and an internal jugular vein occlusion. Metagenomic Next-Generation Sequencing (mNGS) of the alveolar lavage fluid identified Fusobacterium necrophorum, thereby confirming the diagnosis of LS. Intriguingly, the patient exhibited a delayed clinical response despite receiving the appropriate antibiotic. After integrating tigecycline into the treatment to address potential co-infecting bacteria, we observed a marked improvement in his clinical symptoms. Subsequent follow-up over 12 weeks post-discharge revealed complete alleviation of symptoms, and a chest CT scan showed marked regression of the lung lesions.
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  • 文章类型: Case Reports
    坏死梭杆菌(F.坏死)感染在儿科中很少见。此外,血培养对坏死F.的检测时间长,阳性率低。嗜血杆菌感染通常伴随着快速的疾病进展,导致高死亡率。在以前关于坏死F.相关病例的报告中,这种疾病最危险的时刻发生在Lemierre综合征出现之后。我们报告了一例6岁女性患者的非典型病例,该患者在没有Lemierre综合征的情况下,因坏死F.感染而在入院24小时内发生感染性休克。通过宏基因组学下一代测序(mNGS)而不是通过标准血液培养在血液样品中鉴定坏死F.患者在接受及时有效的针对性抗感染治疗后,最终治愈出院。在本案例研究中,据观察,坏死F.的毒力和侵袭性增强对其作为小儿脓毒性休克的主要病原体的作用有重要贡献.这会导致血流动力学不稳定和多器官衰竭,即使没有Lemierre综合征。使用mNGS可以深入快速地识别感染性病原体,指导使用有针对性的抗生素,大大提高了患者的生存率。
    Fusobacterium necrophorum (F. necrophorum) infection is rare in pediatrics. In addition, the detection time of F. necrophorum by blood culture is long, and the positive rate is low. Infection with F. necrophorum bacilli usually follows rapid disease progression, resulting in high mortality. In previous reports of F. necrophorum-related cases, the most dangerous moment of the disease occurred after the appearance of Lemierre\'s syndrome. We report an atypical case of a 6-year-old female patient who developed septic shock within 24 h of admission due to F. necrophorum infection in the absence of Lemierre\'s syndrome. F. necrophorum was identified in a blood sample by metagenomics next-generation sequencing (mNGS) but not by standard blood culture. The patient was finally cured and discharged after receiving timely and effective targeted anti-infection treatment. In the present case study, it was observed that the heightened virulence and invasiveness of F. necrophorum contribute significantly to its role as a primary pathogen in pediatric septic shock. This can precipitate hemodynamic instability and multiple organ failure, even in the absence of Lemierre\'s syndrome. The use of mNGS can deeply and rapidly identify infectious pathogens, guide the use of targeted antibiotics, and greatly improve the survival rate of patients.
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  • 文章类型: Case Reports
    背景:坏死梭杆菌(F.坏死)引起的坏死性肺炎是一种罕见但严重的肺部感染。微生物检测方法不足会导致诊断困难。
    方法:我们报告1例通过支气管肺泡灌洗液(BALF)的下一代测序(NGS)诊断为坏死F.肺脓肿。
    结果:BALF-NGS检测到F。指导后续靶向抗生素治疗。用主动引流和甲硝唑治疗,病人的病情得到有效治疗。
    结论:BALF-NGS是快速诊断由难以培养的细菌引起的感染的有价值的工具。它在坏死F.的早期鉴定中起着决定性的作用,能够及时和有针对性的抗生素干预。早期诊断和适当的治疗对于坏死F.肺炎的治疗至关重要。
    BACKGROUND: Fusobacterium necrophorum (F. necrophorum)-induced necrotizing pneumonia is a rare but severe pulmonary infection. Insufficient microbiological detection methods can lead to diagnostic difficulties.
    METHODS: We report a case of F. necrophorum lung abscess diagnosed by next-generation sequencing (NGS) of bronchoalveolar lavage fluid (BALF).
    RESULTS: BALF-NGS detected F. necrophorum, guiding subsequent targeted antibiotic therapy. With active drainage and metronidazole treatment, the patient\'s condition was effectively treated.
    CONCLUSIONS: BALF-NGS is a valuable tool for the rapid diagnosis of infections caused by difficult-to-culture bacteria. It played a decisive role in the early identification of F. necrophorum, enabling timely and targeted antibiotic intervention. Early diagnosis and appropriate treatment are crucial for the management of F. necrophorum pneumonia.
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  • 文章类型: Case Reports
    背景技术随着抗生素的出现,岩性耳炎(PA),颞骨骨质发炎,已成为中耳炎的罕见并发症。更不常见的是Gradenigo综合征(GS),PA的结果,以中耳炎或化脓性耳漏三联征为特征,由三叉神经的第一和第二部分支配的区域内的疼痛,和同侧外展神经麻痹。最近的文献表明,在GS病例中分离出的坏死梭杆菌的报道越来越多。病例报告一名21岁男子出现耳痛,听力降低,和严重的头痛。检查显示右侧化脓性耳漏,三叉神经内的麻醉分布,和同侧外展神经麻痹。从耳拭子和血液培养物中分离坏死F.。计算机断层扫描和磁共振成像(MRI)显示出耳乳突炎,PA,海绵窦血栓形成,颈内动脉岩性严重狭窄。他接受了静脉注射苄青霉素治疗,接受了乳突切除术并插入了通风管,并开始了为期3个月的达比加群课程。间期MRI显示颈内动脉口径改善,持续性岩尖炎症,和两个海绵状窦的正常外观。随访临床回顾发现持续性外展和三叉神经功能障碍。结论我们确定了190例PA;其中,80与经典的Gradenigo三合会一起呈现。梭杆菌属。在10%的GS病例中培养,使它们成为最常见的隔离物。由于死角的挑剔性质,它在历史文献中可能代表性不足,我们建议经验性抗生素覆盖厌氧生物。
    BACKGROUND With the advent of antibiotics, petrous apicitis (PA), inflammation of the petrous temporal bone, has become a rare complication of otitis media. Even more uncommon is Gradenigo syndrome (GS), a result of PA, characterized by a triad of otitis media or purulent otorrhea, pain within the regions innervated by the first and second division of the trigeminal nerve, and ipsilateral abducens nerve palsy. Recent literature has demonstrated increasing reports of Fusobacterium necrophorum isolated in cases of GS. CASE REPORT A 21-year-old man presented with otalgia, reduced hearing, and severe headache. Examination revealed right-sided purulent otorrhea, anesthesia within the trigeminal nerve distribution, and an ipsilateral abducens nerve palsy. F. necrophorum was isolated from an ear swab and a blood culture. Computed tomography and magnetic resonance imaging (MRI) demonstrated otomastoiditis, PA, cavernous sinus thrombosis, and severe stenosis of the petrous internal carotid artery. He was treated with intravenous benzylpenicillin, underwent a mastoidectomy and insertion of a ventilation tube, and was started on a 3-month course of dabigatran. Interval MRI showed improved internal carotid artery caliber, persistent petrous apex inflammation, and normal appearance of both cavernous sinuses. Follow-up clinical review noted persistent abducens and trigeminal nerve dysfunction. CONCLUSIONS We identified 190 cases of PA; of these, 80 presented with the classic Gradenigo triad. Fusobacterium sp. were cultured in 10% of GS cases, making them the most frequent isolates. Due to the fastidious nature of F. necrophorum, it may be underrepresented in the historical literature, and we recommend that empiric antibiotics cover anaerobic organisms.
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  • 文章类型: Case Reports
    为了了解临床特征,Lemierre综合征(LS)的诊断和治疗,一种高风险和低流行的传染病。
    我们介绍了在我们医院使用宏基因组下一代测序(mNGS)诊断的严重LS病例,并系统总结了2006年至2022年报告LS的患者的诊断和治疗策略。
    我们医院24岁的病人患有脑神经麻痹,在LS病例中很少见的神经系统并发症。病原体(坏死梭杆菌,该患者的Fn)仅通过mNGS测试检测到,随着患者逐渐好转,血浆mNGS检测到的Fn读数减少,表明血浆mNGS在监测治疗疗效方面是有价值的。尽管从文献中检索到的大多数病例都显示出典型的症状,比如喉咙痛的病史,脓毒性栓子,颈内静脉血栓形成,临床表现仍然相对异质(例如,易感因素和病原体的多样性,肺部影像学特征的差异)。
    我们总结了临床表现,诊断,治疗,对17例有症状的病例进行了回归,并报告了LS,为临床医生提供了有关这种罕见但致命的疾病的知识。应尽早考虑进行mNGS检测,以确定可疑感染的急危重症患者的病原体,以实施准确有效的治疗。
    UNASSIGNED: To understand the clinical features, diagnosis and treatment of Lemierre syndrome (LS), a high-risk and low-prevalence infectious disease.
    UNASSIGNED: We present the severe LS case that was diagnosed using metagenomic next-generation sequencing (mNGS) in our hospital, and systematically summarized the diagnosis and treatment strategies of patients that reported LS from 2006 to 2022.
    UNASSIGNED: The 24-year-old patient in our hospital suffered from cranial nerve paralysis, a neurological complication rarely seen in LS cases. The causative agent (Fusobacterium necrophorum, Fn) of this patient was only detected by mNGS tests, and the reads number of Fn detected by plasma mNGS tests was decrease as the patients gradually improved, indicating plasma mNGS is valuable in monitoring treatment efficacy. Although most of the cases retrieved from the literature showed typical symptoms, such as a history of sore throat, septic emboli, and internal jugular vein thrombosis, clinical manifestations were still relatively heterogeneous (eg, diversity of predisposing factors and pathogens, differences in pulmonary imaging features).
    UNASSIGNED: We summarized the clinical presentation, diagnosis, treatment, and regression of 17 symptomatic cases reported LS to provide clinicians with knowledge about this rare but fatal disease. mNGS assays should be considered as early as possible to identify the responsible pathogens for acute and critically ill patients with suspected infections in order to implement accurate and effective treatment.
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  • 文章类型: Case Reports
    Lemierre综合征(LS)是一种罕见且可能危及生命的口咽感染并发症,导致颈内静脉存在化脓性血栓性静脉炎。这种情况最常见的是由坏死梭杆菌引起的,每年每百万人中就有一例。LS更常见于青少年或年轻人,但它也可能发生在儿童身上。尽管它很少发生,这种情况的及时诊断和开始治疗对于预防致命并发症至关重要。在这项研究中,我们报告了一个独特的病例,一个以前健康的7岁男性患有LS,他出现了发烧,左侧颈部疼痛,和肿胀。
    Lemierre\'s syndrome (LS) is a rare and potentially life-threatening complication of an oropharyngeal infection, resulting in the presence of septic thrombophlebitis in the internal jugular vein. This condition is most commonly caused by Fusobacterium necrophorum, with a prevalence of one case per million people annually. LS is more commonly seen in adolescents or young adults, but it can also occur in children. Despite its rare occurrence, prompt diagnosis of this condition and the initiation of treatment are crucial to preventing fatal complications. In this study, we report a unique case of a previously healthy seven-year-old male with LS who presented with fever, left-sided neck pain, and swelling.
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  • 文章类型: Case Reports
    此病例报告说明了坏死梭杆菌引起的Lemierre综合征的独特表现。该病例报告描述了一名20岁的患者,该患者在没有扁桃体炎或口咽部感染的情况下,继发于肩部血肿和颈部脓肿并伴有多种全身并发症。演讲前两周,患者右肩受伤并感染COVID-19。由于他的Lemierre综合征,他出现了右颈内静脉和锁骨下静脉血栓,脓毒性肺栓塞,右侧霍纳综合征,弥散性血管内凝血,骨盆集合,耻骨联合化脓性关节炎和右耻骨骨髓炎,和左股骨干近端。患者接受非手术和手术管理,以管理他的Lemierre综合征,包括手术引流,抗生素,和抗凝;他在长期住院后出院。该病例报告强调了COVID-19阳性患者中罕见的继发于肩部血肿的Lemierre综合征,及其潜在的系统性和危及生命的并发症。它的重要性在COVID-19大流行的背景下高度相关。有必要进行进一步的研究,以探讨先前的COVID-19感染对Lemierre综合征微生物学特征的影响。
    This case report illustrates a unique presentation of Lemierre\'s syndrome precipitated by Fusobacterium necrophorum. This case report describes a 20-year-old patient who developed Lemierre\'s syndrome secondary to a shoulder hematoma and neck abscess with multiple systemic complications in the absence of tonsillitis or oropharyngeal infection. Two weeks prior to presentation, the patient sustained a right shoulder injury and contracted COVID-19. Due to his Lemierre\'s syndrome, he developed right internal jugular vein and subclavian vein thrombosis, septic lung emboli, right sided Horner\'s syndrome, disseminated intravascular coagulation, pelvic collection, septic arthritis of pubic symphysis and osteomyelitis of the right pubic bone, and proximal left femoral shaft. The patient received non-operative and operative management to manage his Lemierre\'s syndrome including surgical drainage, antibiotics, and anticoagulation; he was discharged following an extended hospital stay. This case report highlights a rare presentation of Lemierre\'s syndrome secondary to a shoulder hematoma in a COVID-19 positive patient, and its potential systemic and life-threatening complications. Its importance is highly relevant in the context of the COVID-19 pandemic. Further studies are warranted to explore the effect of preceding COVID-19 infections on the microbiological profile in Lemierre\'s syndrome.
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  • 文章类型: Review
    背景:坏死梭杆菌是一种厌氧菌,革兰氏阴性,不活动,丝状的,在口腔中发现的非孢子形成杆菌,胃肠道,和女性生殖道,导致了一种叫做Lemierre综合症的罕见疾病,以颈内静脉化脓性血栓性静脉炎为特征,这主要影响以前健康的青少年和年轻人;据报道,一些风险因素,如吸烟或原发性病毒或细菌感染导致粘膜破坏。该综合征通常起源于上呼吸道感染,如咽扁桃体炎,急性中耳炎,颈淋巴结炎,鼻窦炎,或者牙源性脓肿,并可能导致多器官转移,更经常导致肺部并发症,尤其是肺脓肿.
    方法:我们描述了在三级护理中心评估的两名患有非典型Lemierre综合征的青少年患者,一个确诊为坏死梭杆菌感染,另一个根据临床特征进行推定诊断,患有肺脓肿的人需要延长抗生素疗程和住院治疗。感兴趣的,都是电子烟的使用者,配置可能的新风险因素。Lemierre综合征的正确诊断通常很难确定,所以需要高度怀疑,特别是在其他健康青少年的肺脓肿的情况下。
    结论:本研究将有助于深入了解青少年Lemierre综合征的临床表现和管理,提高对一种罕见但可能致命的疾病的认识。此外,这表明Lemierre综合征与电子烟的使用之间可能存在关系,这应该由未来的研究进行调查。
    BACKGROUND: Fusobacterium necrophorum is an anaerobic, gram-negative, non-motile, filamentous, non-spore forming bacillus found in the oral cavity, gastrointestinal tract, and female genital tract, responsible of a rare disease named Lemierre Syndrome, characterized by septic thrombophlebitis of the internal jugular vein, which mainly affects previously healthy adolescents and young adults; some risk factors are reported, as smoking or primary viral or bacterial infection leading to the disruption of mucosa. The syndrome originates commonly from an upper respiratory infection such as pharyngotonsillitis, acute otitis media, cervical lymphadenitis, sinusitis, or odontogenic abscess, and may result in multiorgan metastasis, more frequently leading to pulmonary complications, especially lung abscesses.
    METHODS: We describe two cases of adolescents with atypical Lemierre Syndrome evaluated in a tertiary care center, one with a confirmed infection by Fusobacterium necrophorum and one with a presumptive diagnosis based on clinical features, who developed lung abscesses needing a prolonged antibiotic course and hospitalization. Of interest, both were user of electronic cigarette, configuring a possible new risk factor. The proper diagnosis of Lemierre Syndrome is often difficult to establish, so a high degree of suspicion is needed, especially in the case of lung abscesses in otherwise healthy adolescents.
    CONCLUSIONS: The current study will contribute to providing insight into Lemierre Syndrome clinical presentation and management in adolescents, promoting awareness for a rare but potentially fatal disease. Moreover, it suggests a possible relationship between Lemierre syndrome and the use of electronic cigarette, that should be investigated by future studies.
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