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Lemierre syndrome: two cases and a review
Mohammed Iqbal Syed1, David Baring, Michael Addidle
1Department of Otolaryngology, Royal Alexandra Hospital, Paisley, United Kingdom. iqbalms@hotmail.com
The Laryngoscope
|September 1, 2007
Summary
Lemierre syndrome, a serious condition involving internal jugular vein thrombophlebitis, is re-emerging due to decreased awareness and antibiotic resistance. Early diagnosis requires high suspicion despite variable symptoms.
Area of Science:
- Otolaryngology
- Infectious Diseases
- Neurology
Background:
- Lemierre syndrome, often termed the "forgotten disease," is characterized by oropharyngeal infection leading to internal jugular vein thrombophlebitis, septic embolization, and bacteremia, typically caused by Fusobacterium necrophorum.
- The incidence of Lemierre syndrome is increasing, particularly among young adults, coinciding with rising antibiotic resistance and diminished clinical awareness.
Observation:
- This study presents two cases of Lemierre syndrome with diverse and severe presentations, including unusual neurological complications.
- One case exhibited 9th to 12th cranial nerve palsies and Horner syndrome, while the other developed polyneuropathy and a frontal lobe infarct, highlighting the syndrome's varied clinical manifestations.
Findings:
- Diagnosis of Lemierre syndrome can be challenging due to variable clinical features and frequently negative blood cultures.
- The re-emergence of this condition underscores the need for increased vigilance and diagnostic suspicion in clinical practice.
Implications:
- Increased awareness of Lemierre syndrome is crucial for timely diagnosis and management, especially given its potential for severe morbidity and neurological sequelae.
- Further research in otolaryngology journals is warranted to better understand and address this increasingly prevalent infectious disease.