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Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature
INTRODUCTION: Aureobasidium pullulans is a dematiaceous, yeast-like fungus that is ubiquitous in nature and can colonize human hair and skin. It has been implicated clinically as causing skin and soft tissue infections, meningitis, splenic abscesses and peritonitis. We present, to our knowledge, the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Microbiology Society
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982151/ https://www.ncbi.nlm.nih.gov/pubmed/29868175 http://dx.doi.org/10.1099/jmmcr.0.005144 |
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author | Mittal, Jaimie Szymczak, Wendy A. Pirofski, Liise-anne Galen, Benjamin T. |
author_facet | Mittal, Jaimie Szymczak, Wendy A. Pirofski, Liise-anne Galen, Benjamin T. |
author_sort | Mittal, Jaimie |
collection | PubMed |
description | INTRODUCTION: Aureobasidium pullulans is a dematiaceous, yeast-like fungus that is ubiquitous in nature and can colonize human hair and skin. It has been implicated clinically as causing skin and soft tissue infections, meningitis, splenic abscesses and peritonitis. We present, to our knowledge, the second case of isolation of this organism in a patient with AIDS along with a review of the literature on human infection with A. pullulans. CASE PRESENTATION: A 49-year-old man with advanced AIDS and a history of recurrent oesophageal candidiasis was admitted with nausea with vomiting, and odynophagia. He was treated as having a recurrence of oesophageal candidiasis. Given prior Candida albicans isolate susceptibilities and chronic suppression with fluconazole, he was started on micafungin with eventual improvement in his symptoms. A positive blood culture from admission was initially reported to be growing yeast, but four days later the isolate was recognized as a dematiaceous fungus. The final identification of A. pullulans was not available until 1 month after admission. He had completed a 3-week course of micafungin prior to the identification of the isolate, and repeat cultures were negative. CONCLUSION: A. pullulans fungemia is rare but can occur in patients with immune suppression or indwelling catheters. The significance of isolating A. pullulans from a blood culture in terms of whether it is the causative agent of a state of disease often cannot be determined because skin colonization is possible. Further work is needed to clarify the clinical implications of A. pullulans fungemia. |
format | Online Article Text |
id | pubmed-5982151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59821512018-06-04 Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature Mittal, Jaimie Szymczak, Wendy A. Pirofski, Liise-anne Galen, Benjamin T. JMM Case Rep Case Report INTRODUCTION: Aureobasidium pullulans is a dematiaceous, yeast-like fungus that is ubiquitous in nature and can colonize human hair and skin. It has been implicated clinically as causing skin and soft tissue infections, meningitis, splenic abscesses and peritonitis. We present, to our knowledge, the second case of isolation of this organism in a patient with AIDS along with a review of the literature on human infection with A. pullulans. CASE PRESENTATION: A 49-year-old man with advanced AIDS and a history of recurrent oesophageal candidiasis was admitted with nausea with vomiting, and odynophagia. He was treated as having a recurrence of oesophageal candidiasis. Given prior Candida albicans isolate susceptibilities and chronic suppression with fluconazole, he was started on micafungin with eventual improvement in his symptoms. A positive blood culture from admission was initially reported to be growing yeast, but four days later the isolate was recognized as a dematiaceous fungus. The final identification of A. pullulans was not available until 1 month after admission. He had completed a 3-week course of micafungin prior to the identification of the isolate, and repeat cultures were negative. CONCLUSION: A. pullulans fungemia is rare but can occur in patients with immune suppression or indwelling catheters. The significance of isolating A. pullulans from a blood culture in terms of whether it is the causative agent of a state of disease often cannot be determined because skin colonization is possible. Further work is needed to clarify the clinical implications of A. pullulans fungemia. Microbiology Society 2018-03-14 /pmc/articles/PMC5982151/ /pubmed/29868175 http://dx.doi.org/10.1099/jmmcr.0.005144 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article 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 the original author and source are credited. |
spellingShingle | Case Report Mittal, Jaimie Szymczak, Wendy A. Pirofski, Liise-anne Galen, Benjamin T. Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature |
title | Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature |
title_full | Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature |
title_fullStr | Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature |
title_full_unstemmed | Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature |
title_short | Fungemia caused by Aureobasidium pullulans in a patient with advanced AIDS: a case report and review of the medical literature |
title_sort | fungemia caused by aureobasidium pullulans in a patient with advanced aids: a case report and review of the medical literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982151/ https://www.ncbi.nlm.nih.gov/pubmed/29868175 http://dx.doi.org/10.1099/jmmcr.0.005144 |
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