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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Main Authors: Mridul Gupta, Radhika Annam, Joseph Bahgat, Margaret Eng
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Case Reports in Infectious Diseases
Online Access:http://dx.doi.org/10.1155/2018/3628395
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spelling 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
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