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Atypical presentation of Lemierre’s syndrome: case report and literature review
BACKGROUND: The classic Lemierre’s syndrome refers to a septic thrombosis of the internal jugular vein, usually caused by a Fusobacterium necrophorum infection starting in the oral cavity, and typically complicated by pulmonary emboli. However, unusual forms of the disorder have been rarely reported...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805316/ https://www.ncbi.nlm.nih.gov/pubmed/31638919 http://dx.doi.org/10.1186/s12879-019-4538-6 |
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author | Laurencet, Marie-Eva Rosset--Zufferey, Sarah Schrenzel, Jacques |
author_facet | Laurencet, Marie-Eva Rosset--Zufferey, Sarah Schrenzel, Jacques |
author_sort | Laurencet, Marie-Eva |
collection | PubMed |
description | BACKGROUND: The classic Lemierre’s syndrome refers to a septic thrombosis of the internal jugular vein, usually caused by a Fusobacterium necrophorum infection starting in the oral cavity, and typically complicated by pulmonary emboli. However, unusual forms of the disorder have been rarely reported. CASE PRESENTATION: We describe an unusual case of a previously healthy 58-year-old male with Lemierre’s syndrome, manifesting with lumbar pain and fever. A thrombosis of the iliac veins and abscesses in the right iliac and the left psoas muscles was diagnosed by a computed tomography scan, together with a right lung pneumonia complicated by pleural effusion and an L4-L5 spondylodiscitis. Blood culture and pus drainage were positive for Fusobacterium nucleatum and an atypical Lemierre’s syndrome was suspected. The patient was treated with anticoagulant therapy for 12 weeks and intravenous antibiotic therapy for 6 weeks with a good evolution and resolution of the thrombosis. CONCLUSIONS: This case illustrates the thrombogenic and thromboembolic tendency of Fusobacterium nucleatum and its potential invasiveness, regardless of the site of primary infection. The concept of an atypical Lemierre’s syndrome is redefined here to take into consideration non-cervical sites. |
format | Online Article Text |
id | pubmed-6805316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68053162019-10-24 Atypical presentation of Lemierre’s syndrome: case report and literature review Laurencet, Marie-Eva Rosset--Zufferey, Sarah Schrenzel, Jacques BMC Infect Dis Case Report BACKGROUND: The classic Lemierre’s syndrome refers to a septic thrombosis of the internal jugular vein, usually caused by a Fusobacterium necrophorum infection starting in the oral cavity, and typically complicated by pulmonary emboli. However, unusual forms of the disorder have been rarely reported. CASE PRESENTATION: We describe an unusual case of a previously healthy 58-year-old male with Lemierre’s syndrome, manifesting with lumbar pain and fever. A thrombosis of the iliac veins and abscesses in the right iliac and the left psoas muscles was diagnosed by a computed tomography scan, together with a right lung pneumonia complicated by pleural effusion and an L4-L5 spondylodiscitis. Blood culture and pus drainage were positive for Fusobacterium nucleatum and an atypical Lemierre’s syndrome was suspected. The patient was treated with anticoagulant therapy for 12 weeks and intravenous antibiotic therapy for 6 weeks with a good evolution and resolution of the thrombosis. CONCLUSIONS: This case illustrates the thrombogenic and thromboembolic tendency of Fusobacterium nucleatum and its potential invasiveness, regardless of the site of primary infection. The concept of an atypical Lemierre’s syndrome is redefined here to take into consideration non-cervical sites. BioMed Central 2019-10-21 /pmc/articles/PMC6805316/ /pubmed/31638919 http://dx.doi.org/10.1186/s12879-019-4538-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Laurencet, Marie-Eva Rosset--Zufferey, Sarah Schrenzel, Jacques Atypical presentation of Lemierre’s syndrome: case report and literature review |
title | Atypical presentation of Lemierre’s syndrome: case report and literature review |
title_full | Atypical presentation of Lemierre’s syndrome: case report and literature review |
title_fullStr | Atypical presentation of Lemierre’s syndrome: case report and literature review |
title_full_unstemmed | Atypical presentation of Lemierre’s syndrome: case report and literature review |
title_short | Atypical presentation of Lemierre’s syndrome: case report and literature review |
title_sort | atypical presentation of lemierre’s syndrome: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805316/ https://www.ncbi.nlm.nih.gov/pubmed/31638919 http://dx.doi.org/10.1186/s12879-019-4538-6 |
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