Lemierre syndrome (LS) is a rapidly progressing disease characterised by a recent oropharyngeal infection, complicated by septic emboli and thrombophlebitis of the internal jugular vein (IJV). We describe a case of a 65-year-old woman who presented to the emergency room with a 14-day history of progressive occipital headache, fever and odynophagia. Radiological investigations showed bilateral IJV thrombophlebitis, multiple cavitated pulmonary nodules suggestive of septic emboli and a subsegmental pulmonary arterial thromboembolism. A diagnosis of LS was made. The patient received antibiotic treatment with intravenous ceftriaxone and clindamycin for 2 weeks, followed by 4 weeks of oral clindamycin at home and anticoagulation with enoxaparin followed by warfarin. One-month follow-up imaging revealed complete resolution of IJV thrombosis and pulmonary findings. This case displayed the rarely reported association of pulmonary arterial thromboembolism and pulmonary septic emboli.
Association of pulmonary septic embolism and pulmonary arterial thromboembolism in Lemierre syndrome. A case report and literature review / Fabozzi, Antonio; Siena, Alessandro; Steffanina, Alessia; Iannuzzi, Silvia; Bonini, Matteo; Palange, Paolo. - In: RESPIROLOGY CASE REPORTS. - ISSN 2051-3380. - 13:7(2025), pp. 1-4. [10.1002/rcr2.70266]
Association of pulmonary septic embolism and pulmonary arterial thromboembolism in Lemierre syndrome. A case report and literature review
Fabozzi, Antonio
Primo
;Siena, Alessandro;Steffanina, Alessia;Iannuzzi, Silvia;Bonini, Matteo;Palange, Paolo
2025
Abstract
Lemierre syndrome (LS) is a rapidly progressing disease characterised by a recent oropharyngeal infection, complicated by septic emboli and thrombophlebitis of the internal jugular vein (IJV). We describe a case of a 65-year-old woman who presented to the emergency room with a 14-day history of progressive occipital headache, fever and odynophagia. Radiological investigations showed bilateral IJV thrombophlebitis, multiple cavitated pulmonary nodules suggestive of septic emboli and a subsegmental pulmonary arterial thromboembolism. A diagnosis of LS was made. The patient received antibiotic treatment with intravenous ceftriaxone and clindamycin for 2 weeks, followed by 4 weeks of oral clindamycin at home and anticoagulation with enoxaparin followed by warfarin. One-month follow-up imaging revealed complete resolution of IJV thrombosis and pulmonary findings. This case displayed the rarely reported association of pulmonary arterial thromboembolism and pulmonary septic emboli.| File | Dimensione | Formato | |
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