Abstract: n otherwise healthy 16-year-old female was transferred to Children’s Hospital from a community hospital 12 days after she began experiencing sore throat, intermittent fevers, vomiting, and diarrhea. She was initially treated conservatively for suspected flu symptoms, but her condition continued to worsen with progressive sore throat, dysphagia, decreased appetite, cough, and fevers approaching 104.5°F. She was admitted to a community hospital for treatment of suspected community-acquired pneumonia based upon the presence of multilobar air space disease on chest radiographs. Despite aggressive monitoring and treatment, her condition continued to deteriorate.
On arrival at Children’s Hospital the patient was hypotensive, tachycardic, tachypneic, and febrile. Physical examination demonstrated an erythematous oropharynx with slight tonsillar prominence on the right. There were no appreciable exudates. Lung auscultation revealed bilateral crackles. Laboratory findings were significant for an elevated white blood cell count with a left shift. Contrast-enhanced computed tomography (CT) examination of the neck and chest was subsequently performed.
Based upon the patient’s clinical symptoms and radiographic findings, the diagnosis of Lemierre’s syndrome was suspected and later confirmed with blood cultures positive for Fusobacterium necrophorum. With close monitoring, appropriate antibiotic therapy, and incision and drainage of the peritonsillar abscess, the patient achieved a full recovery.
The views expressed in this material are those of the authors, and do not reflect the official policy or position of the U.S. Government, the Department of Defense, or the Department of the Air Force.
Contrast-enhanced CT of the neck and chest revealed a large right-sided peritonsillar abscess (Figure 1), thrombus along the anterior aspect of the right internal jugular vein (Figure 2), and multiple septic pulmonary emboli (Figure 3).
Lemierre’s syndrome is a rare clinical entity with fewer than 160 cases reported since it was first described in the early 1900’s.1 The syndrome consists of internal jugular venous thrombosis following a primary oropharyngeal infection with development of distant septic emboli.2 The lungs are nearly always affected; however, any organ system may be involved. Recent literature suggests that there may be a resurgence of this rare entity due to more prudent use of antibiotics in treatment of sore throat.3
Lemierre’s syndrome classically occurs in otherwise healthy adolescents and young adults. Patients present with sepsis after an antecedent oropharyngeal infection. Diagnosis is often delayed due to the indolent nature of the infection and the obscurity of the disease.4 The causative organism in the vast majority of cases is F. necrophorum, an anaerobic bacteria that is part of the normal flora of the oropharynx, but is capable of producing toxins that can dissect fascial planes and stimulate platelet aggregation. Diagnosis is made with positive blood cultures combined with appropriate imaging findings. Imaging findings include internal jugular venous thrombosis and the detection of distant emboli, usually within the lungs. Often, the imaging findings precede clinical suspicion and blood culture results; therefore, radiologists play a crucial role in early recognition of this syndrome.5
Once properly diagnosed, treatment includes antibiotics tailored to susceptibility analyses and drainage of any loculated infectious fluid collections. Supportive care for respiratory or hemodynamic collapse is essential and intensive care monitoring is preferred. The use of anticoagulation in the treatment of jugular venous thrombosis is debated, since anticoagulation may actually propagate the infection. Only with prompt diagnosis and treatment may a full recovery be possible.
The imaging modalities used to diagnose Lemierre’s syndrome vary based upon the clinical scenario. Ultrasound, CT, and magnetic resonance imaging (MRI) have all proven beneficial. For the evaluation of septic pulmonary emboli, CT has proven to be the imaging modality of choice. With regard to internal jugular venous thrombosis, all 3 modalities have their advantages and limitations, however, ultrasound is often the initial imaging modality of choice due to its availability and lack of ionizing radiation.6 MRI also lacks ionizing radiation, however, sedation is often necessary to complete the study. Contrast-enhanced CT is commonly used for evaluation of internal jugular venous thrombosis, especially when performed in conjunction with a chest CT to evaluate for septic pulmonary emboli.
Lemierre’s syndrome is a rare and potentially lethal entity affecting otherwise healthy adolescents and young adults. It consists of internal jugular venous thrombosis following a primary oropharyngeal infection with development of distant septic emboli, most often involving the lungs. Prompt diagnosis and treatment are necessary to prevent sepsis and subsequent death. Often, imaging findings precede clinical suspicion and blood culture results, therefore, the role of radiologists is crucial to the early recognition of this syndrome.
- 1. Sara Z, Beard G, Furey W. Insight into a forgotten disease: Lemierre’s syndrome. Resid Staff Physician. 2005;51:37-40.
- Riordan T, Wilson M. Lemierre’s syndrome: more than a historical curiosa. Postgrad Med J. 2004;23:241-245.
- Kristensen LH, Prag J. Human necrobacillus, with emphasis on Lemierre’s syndrome. Clin Infect Dis. 2000;31:524-532.
- Engelke C, Rummeny EJ, Marten K. A patient with prolonged fever after pharyngotonsillitis. Br J Radiol. 2004;77:627-628.
- Screaton NJ, Ravenel JG, Lehner PJ, et al. Lemierre syndrome: Forgotten but not extinct —report of four cases. Radiology. 1999;213:369-374.
- De Lima JE Jr, Levin M. Lemierre’s syndrome: Post-anginal septicemia. Pediatr Radiol. 2003;33:281-283.