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Scedosporium apiospermum as a rare cause of central skull base osteomyelitis
We report a case of Scedosporium apiospermum mold causing ear infection, central skull base osteomyelitis and finally, occlusion of carotid artery in a 48-year-old diabetic man. The exact diagnosis was established and the severity of the disease understood several months after the onset of symptoms....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834721/ https://www.ncbi.nlm.nih.gov/pubmed/27134821 http://dx.doi.org/10.1016/j.mmcr.2016.04.002 |
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author | Jalava-Karvinen, Päivi Nyman, Mikko Gardberg, Maria Harju, Inka Hohenthal, Ulla Oksi, Jarmo |
author_facet | Jalava-Karvinen, Päivi Nyman, Mikko Gardberg, Maria Harju, Inka Hohenthal, Ulla Oksi, Jarmo |
author_sort | Jalava-Karvinen, Päivi |
collection | PubMed |
description | We report a case of Scedosporium apiospermum mold causing ear infection, central skull base osteomyelitis and finally, occlusion of carotid artery in a 48-year-old diabetic man. The exact diagnosis was established and the severity of the disease understood several months after the onset of symptoms. Despite of appropriate antifungal therapy, and repeated surgical and otological procedures, the infection progressed to fatal cerebral infarction. |
format | Online Article Text |
id | pubmed-4834721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48347212016-04-29 Scedosporium apiospermum as a rare cause of central skull base osteomyelitis Jalava-Karvinen, Päivi Nyman, Mikko Gardberg, Maria Harju, Inka Hohenthal, Ulla Oksi, Jarmo Med Mycol Case Rep Case Report We report a case of Scedosporium apiospermum mold causing ear infection, central skull base osteomyelitis and finally, occlusion of carotid artery in a 48-year-old diabetic man. The exact diagnosis was established and the severity of the disease understood several months after the onset of symptoms. Despite of appropriate antifungal therapy, and repeated surgical and otological procedures, the infection progressed to fatal cerebral infarction. Elsevier 2016-04-07 /pmc/articles/PMC4834721/ /pubmed/27134821 http://dx.doi.org/10.1016/j.mmcr.2016.04.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Jalava-Karvinen, Päivi Nyman, Mikko Gardberg, Maria Harju, Inka Hohenthal, Ulla Oksi, Jarmo Scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
title | Scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
title_full | Scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
title_fullStr | Scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
title_full_unstemmed | Scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
title_short | Scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
title_sort | scedosporium apiospermum as a rare cause of central skull base osteomyelitis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834721/ https://www.ncbi.nlm.nih.gov/pubmed/27134821 http://dx.doi.org/10.1016/j.mmcr.2016.04.002 |
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