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Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature
Haemophilus parainfluenzae, which uncommonly causes endocarditis, has never been documented to cause mural involvement. A 62-year-old immunocompetent female without predisposing risk factors for endocarditis except for poor dentition presented with fever, emesis, and dysmetria. Echocardiography foun...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921150/ https://www.ncbi.nlm.nih.gov/pubmed/27382494 http://dx.doi.org/10.1155/2016/3639517 |
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author | Giurgea, Luca T. Lahey, Tim |
author_facet | Giurgea, Luca T. Lahey, Tim |
author_sort | Giurgea, Luca T. |
collection | PubMed |
description | Haemophilus parainfluenzae, which uncommonly causes endocarditis, has never been documented to cause mural involvement. A 62-year-old immunocompetent female without predisposing risk factors for endocarditis except for poor dentition presented with fever, emesis, and dysmetria. Echocardiography found a mass attached to the left ventricular wall with finger-like projections. Computed tomography showed evidence of embolic phenomena to the brain, kidneys, spleen, and colon. Cardiac MRI revealed involvement of the chordae tendineae of the anterior papillary muscles. Blood cultures grew Haemophilus parainfluenzae. The patient was treated successfully with ceftriaxone with resolution of symptoms, including neurologic deficits. After eleven days of antibiotics a worsening holosystolic murmur was discovered. Worsening mitral regurgitation on echocardiography was only found three weeks later. Nine weeks after presentation, intraoperative evaluation revealed chord rupture but no residual vegetation and mitral repair was performed. Four weeks after surgery, the patient was back to her baseline. This case illustrates the ability of Haemophilus parainfluenzae to form large mural vegetations with high propensity of embolization in otherwise normal cardiac tissue among patients with dental risk factors. It also underscores the importance of physical examination in establishing a diagnosis of endocarditis and monitoring for progression of disease. |
format | Online Article Text |
id | pubmed-4921150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49211502016-07-05 Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature Giurgea, Luca T. Lahey, Tim Case Rep Infect Dis Case Report Haemophilus parainfluenzae, which uncommonly causes endocarditis, has never been documented to cause mural involvement. A 62-year-old immunocompetent female without predisposing risk factors for endocarditis except for poor dentition presented with fever, emesis, and dysmetria. Echocardiography found a mass attached to the left ventricular wall with finger-like projections. Computed tomography showed evidence of embolic phenomena to the brain, kidneys, spleen, and colon. Cardiac MRI revealed involvement of the chordae tendineae of the anterior papillary muscles. Blood cultures grew Haemophilus parainfluenzae. The patient was treated successfully with ceftriaxone with resolution of symptoms, including neurologic deficits. After eleven days of antibiotics a worsening holosystolic murmur was discovered. Worsening mitral regurgitation on echocardiography was only found three weeks later. Nine weeks after presentation, intraoperative evaluation revealed chord rupture but no residual vegetation and mitral repair was performed. Four weeks after surgery, the patient was back to her baseline. This case illustrates the ability of Haemophilus parainfluenzae to form large mural vegetations with high propensity of embolization in otherwise normal cardiac tissue among patients with dental risk factors. It also underscores the importance of physical examination in establishing a diagnosis of endocarditis and monitoring for progression of disease. Hindawi Publishing Corporation 2016 2016-06-12 /pmc/articles/PMC4921150/ /pubmed/27382494 http://dx.doi.org/10.1155/2016/3639517 Text en Copyright © 2016 L. T. Giurgea and T. Lahey. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Giurgea, Luca T. Lahey, Tim Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature |
title |
Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature |
title_full |
Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature |
title_fullStr |
Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature |
title_full_unstemmed |
Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature |
title_short |
Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature |
title_sort | haemophilus parainfluenzae mural endocarditis: case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921150/ https://www.ncbi.nlm.nih.gov/pubmed/27382494 http://dx.doi.org/10.1155/2016/3639517 |
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