Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville 37232-4700, TN, USA.
Am J Emerg Med. 2013 Jan;31(1):274.e5-7. doi: 10.1016/j.ajem.2012.05.019. Epub 2012 Jul 16.
Lemierre syndrome is a potentially life-threatening septic thrombophlebitis associated with a neck infection. We present a case of a 10-month-old female infant with Lemierre syndrome complicated by thrombotic strokes and purulent pericarditis. A healthy 10-month-old female infant presented to the pediatric emergency department of our tertiary care center complaining of 5 days of fever to 105°F and 1 day of neck stiffness and decreased oral intake. In the pediatric emergency department, she developed septic shock, requiring vasopressor support, endotracheal intubation, and broad-spectrum antibiotics. A computed tomographic scan demonstrated a neck abscess associated with a right internal jugular thrombus and septic emboli to her lungs and brain. This constellation was consistent with Lemierre syndrome. Further studies demonstrated the thrombus extended into her left ventricular outflow tract. She was emergently taken to the operating room for incision and drainage of her neck abscess, started on anticoagulation with heparin, and eventually transitioned to enoxaparin. Her hospital course was complicated by a middle cerebral artery distribution infarction and subsequent hemorrhagic conversion with generalized tonic clonic seizures managed by levetiracetam. Ten days into her hospital stay, she developed pericardial tamponade, and cardiac surgery performed a pericardial window for loculated, purulent pericardial effusion. Initial blood cultures were positive for methicillin-sensitive Staphylococcus aureus, and the patient was treated with 6 weeks of nafcillin. She has recovered with minimal permanent sequelae. This is one of the youngest cases of Lemierre syndrome documented. To our knowledge, it is also the first case complicated by purulent pericarditis reported in the literature.
利氏综合征是一种潜在危及生命的与颈部感染相关的脓毒性血栓性静脉炎。我们报告了一例 10 个月大的女性婴儿患利氏综合征,并发血栓性中风和化脓性心包炎。一名 10 个月大的健康女婴因发热至 105°F 5 天、颈部僵硬和摄食量减少而到我们的三级保健中心儿科急诊就诊。在儿科急诊室,她发生了感染性休克,需要血管加压药支持、气管插管和广谱抗生素。计算机断层扫描显示颈部脓肿伴右颈内静脉血栓形成和脓毒性栓子至肺部和大脑。这种组合符合利氏综合征的特征。进一步的研究表明血栓延伸至她的左心室流出道。她被紧急送往手术室进行颈部脓肿切开引流,开始用肝素进行抗凝治疗,最终转为依诺肝素。她的住院过程中出现大脑中动脉分布梗死,随后出现全身强直阵挛性癫痫,用左乙拉西坦治疗出血性转化。住院 10 天后,她出现心包填塞,心脏外科手术进行心包开窗术,以排出局限性化脓性心包积液。初始血培养阳性为甲氧西林敏感金黄色葡萄球菌,患者接受了 6 周的萘夫西林治疗。她已康复,仅有轻微的永久性后遗症。这是有记录以来最年轻的利氏综合征病例之一。据我们所知,这也是文献中首次报告并发化脓性心包炎的病例。