Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome
Lemierre’s syndrome is a rare disease associated with significant morbidity and mortality. It begins with an oropharyngeal infection, which spreads locally to involve the internal jugular vein causing thrombophlebitis, followed by distant spread and metastatic infections. Affected individuals are co...
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2018-01-01
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Series: | Case Reports in Infectious Diseases |
Online Access: | http://dx.doi.org/10.1155/2018/3628395 |
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doaj-0126adaf5ce34cf888672c2758bb937e2020-11-24T20:56:11ZengHindawi LimitedCase Reports in Infectious Diseases2090-66252090-66332018-01-01201810.1155/2018/36283953628395Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s SyndromeMridul Gupta0Radhika Annam1Joseph Bahgat2Margaret Eng3Internal Medicine, Monmouth Medical Center, Long Branch, NJ, USAInternal Medicine, Monmouth Medical Center, Long Branch, NJ, USASt. George’s University, West Indies, GrenadaInternal Medicine, Monmouth Medical Center, Long Branch, NJ, USALemierre’s syndrome is a rare disease associated with significant morbidity and mortality. It begins with an oropharyngeal infection, which spreads locally to involve the internal jugular vein causing thrombophlebitis, followed by distant spread and metastatic infections. Affected individuals are commonly young adults. Causative organisms are usually oropharyngeal flora, most commonly being the anaerobe Fusobacterium necrophorum. Porphyromonas asaccharolytica is a rare etiological agent with only three cases being reported in the literature. This case report describes a previously healthy 22-year-old man who initially presented with acute tonsillitis and was later found to have left internal jugular vein thrombophlebitis along with bilateral septic emboli to the lungs. The patient was treated with a five-week course of ampicillin-sulbactam and metronidazole. Subsequent imaging also showed progression of internal jugular vein thrombus, for which warfarin was given for three months for anticoagulation.http://dx.doi.org/10.1155/2018/3628395 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mridul Gupta Radhika Annam Joseph Bahgat Margaret Eng |
spellingShingle |
Mridul Gupta Radhika Annam Joseph Bahgat Margaret Eng Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome Case Reports in Infectious Diseases |
author_facet |
Mridul Gupta Radhika Annam Joseph Bahgat Margaret Eng |
author_sort |
Mridul Gupta |
title |
Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome |
title_short |
Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome |
title_full |
Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome |
title_fullStr |
Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome |
title_full_unstemmed |
Porphyromonas asaccharolytica as a Rare Causative Agent for Lemierre’s Syndrome |
title_sort |
porphyromonas asaccharolytica as a rare causative agent for lemierre’s syndrome |
publisher |
Hindawi Limited |
series |
Case Reports in Infectious Diseases |
issn |
2090-6625 2090-6633 |
publishDate |
2018-01-01 |
description |
Lemierre’s syndrome is a rare disease associated with significant morbidity and mortality. It begins with an oropharyngeal infection, which spreads locally to involve the internal jugular vein causing thrombophlebitis, followed by distant spread and metastatic infections. Affected individuals are commonly young adults. Causative organisms are usually oropharyngeal flora, most commonly being the anaerobe Fusobacterium necrophorum. Porphyromonas asaccharolytica is a rare etiological agent with only three cases being reported in the literature. This case report describes a previously healthy 22-year-old man who initially presented with acute tonsillitis and was later found to have left internal jugular vein thrombophlebitis along with bilateral septic emboli to the lungs. The patient was treated with a five-week course of ampicillin-sulbactam and metronidazole. Subsequent imaging also showed progression of internal jugular vein thrombus, for which warfarin was given for three months for anticoagulation. |
url |
http://dx.doi.org/10.1155/2018/3628395 |
work_keys_str_mv |
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1716790436745445376 |