Not Forgotten by Novel Disease: COVID-19 Complicated by Lemierre’s Syndrome

J. Wang, S. Young
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Abstract

Introduction: Lemierre's syndrome is an extremely rare disease that generally occurs in young, healthy adults and is characterized by oropharyngeal infection followed by septic thrombophlebitis of the internal jugular vein. We present a case of COVID-19 infection complicated by acute mastoiditis with concomitant Lemierre's syndrome. Case Presentation: A 57-year-old male with obesity and asthma presented with worsening dyspnea after diagnosis of COVID-19 three days prior. The patient was febrile to 101 degrees Fahrenheit and hypoxemic requiring 15 liters supplemental oxygen. CT chest showed severe multifocal bilateral pulmonary opacities and initial blood cultures were negative. He received dexamethasone, remdesivir, and convalescent plasma but clinical status deteriorated with progression of respiratory and renal failure. The patient was eventually intubated and a left internal jugular central venous catheter was placed for renal replacement therapy. Hospital course was further complicated by new onset atrial fibrillation with RVR, for which amiodarone and heparin infusions were started. Four days later, the patient developed intermittent fevers and was found to have Fusobacterium nucleatum bacteremia. Doppler ultrasound showed thrombosis of the left internal jugular vein consistent with Lemierre's syndrome. Physical exam did not exhibit neck edema, induration or dental infection, but CT head and chest revealed acute bilateral mastoiditis and new right upper lobe abscess. Despite removal of internal jugular venous catheter, continued anticoagulation, and initiation of broad spectrum antibiotics, the patient developed worsening multiorgan failure and septic shock requiring vasopressors. He ultimately underwent PEA arrest and did not survive resuscitation. Discussion: Lemierre's syndrome is a rare condition with an estimated worldwide incidence of one in 1 million and a high mortality between 5% to 18%. The most common pathogen is Fusobacterium necrophorum. Moreover, our patient had elevated risk of thrombosis from COVID-19 and a recently placed central venous catheter. As providers increasingly care for patients with COVID-19, early recognition and management of this rare complication is paramount to reduce mortality. Fusobacterium bacteremia should lead to a high index of suspicion for timely diagnosis and treatment of Lemierre's syndrome.
不被新疾病遗忘:COVID-19合并莱米尔综合征
Lemierre综合征是一种极其罕见的疾病,通常发生在年轻健康的成年人中,其特征是口咽感染,然后是颈内静脉脓毒性血栓性静脉炎。我们报告一例COVID-19感染并发急性乳突炎并伴有Lemierre综合征。病例介绍:一名57岁男性,患有肥胖和哮喘,在诊断COVID-19三天前出现呼吸困难加重。病人高烧到101华氏度,低氧需要补充15升氧气。胸部CT显示严重的双侧多灶性肺混浊,初始血培养呈阴性。患者接受了地塞米松、瑞德西韦和恢复期血浆治疗,但随着呼吸和肾功能衰竭的进展,临床状况恶化。患者最终插管并放置左颈内中心静脉导管进行肾脏替代治疗。新发房颤合并RVR使住院过程进一步复杂化,并开始胺碘酮和肝素输注。4天后,患者出现间歇性发热,并发现有核梭杆菌菌血症。多普勒超声显示左颈内静脉血栓形成符合勒米尔综合征。体格检查未发现颈部水肿、硬化或牙齿感染,但头部和胸部CT显示急性双侧乳突炎和新的右上肺叶脓肿。尽管取出颈内静脉导管,继续抗凝治疗,并开始使用广谱抗生素,但患者出现了越来越严重的多器官衰竭和感染性休克,需要血管加压药物。他最终进行了PEA骤停,并没有在复苏中存活下来。讨论:Lemierre综合征是一种罕见的疾病,据估计全球发病率为百万分之一,死亡率在5%至18%之间。最常见的病原体是坏死梭杆菌。此外,我们的患者因COVID-19而血栓形成的风险增加,并且最近放置了中心静脉导管。随着医护人员越来越多地照顾COVID-19患者,早期识别和管理这一罕见并发症对于降低死亡率至关重要。梭杆菌菌血症应引起高度怀疑,以便及时诊断和治疗莱米尔综合征。
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