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An Unusual Case of Modified Lemierre’s Syndrome Caused by Staphylococcus aureus Cellulitis

Patient: Male, 31-year-old Final Diagnosis: Lemierre’s Disease Symptoms: Conjunctival injection • eye pain and redness • fever • nasal swelling • periorbital oedema • ptosis • vesicular lesions nose Medication: — Clinical Procedure: None Specialty: Infectious Diseases OBJECTIVE: Rare disease BACKGRO...

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Detalles Bibliográficos
Autores principales: Elhakeem, Israa A., Al Shokri, Shaikha D., Elzouki, Abdul-Naser Y., Danjuma, Mohammed I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017838/
https://www.ncbi.nlm.nih.gov/pubmed/32008035
http://dx.doi.org/10.12659/AJCR.916575
Descripción
Sumario:Patient: Male, 31-year-old Final Diagnosis: Lemierre’s Disease Symptoms: Conjunctival injection • eye pain and redness • fever • nasal swelling • periorbital oedema • ptosis • vesicular lesions nose Medication: — Clinical Procedure: None Specialty: Infectious Diseases OBJECTIVE: Rare disease BACKGROUND: Lemierre’s syndrome is a potential life-threatening disease commonly occurring in young, healthy individuals. It is often preceded by an oropharyngeal infection causing bacteremia. This may rapidly progress into thrombophlebitis of the internal jugular venous system, its branches, and septic embolization and often fulminant organ failure. CASE REPORT: A previously healthy 31-year-old male with recent history of facial herpes zoster infection, presented with 1-week history of increasingly painful nasal, and periorbital swelling. Imaging confirmed superior ophthalmic vein thrombosis. Staphylococcus aureus was isolated in blood cultures and had an uncomplicated hospital course with full recovery. CONCLUSIONS: Early recognition of Lemierre’s syndrome contributes significantly in reducing morbidity and mortality associated with it. Staphylococcus aureus skin infection is a very rare cause of Lemierre’s syndrome, and its association with superior ophthalmic vein thrombosis has not yet been reported in literature.