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A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings
BACKGROUND : Histoplasma capsulatum is an extremely rare cause of prosthetic valve endocarditis (PVE) and can present with non-specific symptoms leading to a delay in diagnosis with unfavourable outcomes. CASE SUMMARY : A 65-year-old male patient with a history of a bioprosthetic aortic valve replac...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764570/ https://www.ncbi.nlm.nih.gov/pubmed/31660498 http://dx.doi.org/10.1093/ehjcr/ytz127 |
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author | Adigun, Rosalyn O Baddour, Larry M Geske, Jeffrey B |
author_facet | Adigun, Rosalyn O Baddour, Larry M Geske, Jeffrey B |
author_sort | Adigun, Rosalyn O |
collection | PubMed |
description | BACKGROUND : Histoplasma capsulatum is an extremely rare cause of prosthetic valve endocarditis (PVE) and can present with non-specific symptoms leading to a delay in diagnosis with unfavourable outcomes. CASE SUMMARY : A 65-year-old male patient with a history of a bioprosthetic aortic valve replacement and non-obstructive coronary artery disease was admitted for altered mentation, failure to thrive, and a 20-pound unintentional weight loss over the past 4 months. Upon examination, he was lethargic but afebrile and haemodynamically stable. A late peaking ejection murmur was heard on exam. Skin exam was significant for embolic phenomenon involving the extremities. Inflammatory markers and serum calcium were elevated. A bedside echocardiogram showed severe obstruction across the aortic valve prosthesis. Two years prior, he had an echocardiogram with a normal functioning prosthesis. Routine blood cultures were negative and serologic screening was unrevealing. Urine Histoplasma antigen screen was positive on hospital day 3 and on hospital day 10, fungal blood cultures were positive for H. capsulatum. Unfortunately, the patient died shortly afterwards as a result of multiorgan failure from embolic manifestations of the infection. DISCUSSION : Based on our patient's findings and those of previously reported cases in the literature, H. capsulatum PVE should be strongly considered in patients from endemic areas with non-specific symptoms and negative routine blood cultures. |
format | Online Article Text |
id | pubmed-6764570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67645702019-10-02 A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings Adigun, Rosalyn O Baddour, Larry M Geske, Jeffrey B Eur Heart J Case Rep Case Reports BACKGROUND : Histoplasma capsulatum is an extremely rare cause of prosthetic valve endocarditis (PVE) and can present with non-specific symptoms leading to a delay in diagnosis with unfavourable outcomes. CASE SUMMARY : A 65-year-old male patient with a history of a bioprosthetic aortic valve replacement and non-obstructive coronary artery disease was admitted for altered mentation, failure to thrive, and a 20-pound unintentional weight loss over the past 4 months. Upon examination, he was lethargic but afebrile and haemodynamically stable. A late peaking ejection murmur was heard on exam. Skin exam was significant for embolic phenomenon involving the extremities. Inflammatory markers and serum calcium were elevated. A bedside echocardiogram showed severe obstruction across the aortic valve prosthesis. Two years prior, he had an echocardiogram with a normal functioning prosthesis. Routine blood cultures were negative and serologic screening was unrevealing. Urine Histoplasma antigen screen was positive on hospital day 3 and on hospital day 10, fungal blood cultures were positive for H. capsulatum. Unfortunately, the patient died shortly afterwards as a result of multiorgan failure from embolic manifestations of the infection. DISCUSSION : Based on our patient's findings and those of previously reported cases in the literature, H. capsulatum PVE should be strongly considered in patients from endemic areas with non-specific symptoms and negative routine blood cultures. Oxford University Press 2019-09-17 /pmc/articles/PMC6764570/ /pubmed/31660498 http://dx.doi.org/10.1093/ehjcr/ytz127 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Reports Adigun, Rosalyn O Baddour, Larry M Geske, Jeffrey B A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
title | A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
title_full | A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
title_fullStr | A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
title_full_unstemmed | A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
title_short | A case report of Histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
title_sort | case report of histoplasma capsulatum prosthetic valve endocarditis: an extremely rare presentation with characteristic findings |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764570/ https://www.ncbi.nlm.nih.gov/pubmed/31660498 http://dx.doi.org/10.1093/ehjcr/ytz127 |
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