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Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate

The Alternaria species are dematiaceous fungi. Human infection due to dematiaceous fungi is uncommon. Most reported cases of alternariosis have occurred in patients with immunodeficiency. The majority of cases were solid-organ transplantation recipients. Cutaneous alternariosis lesions are usually a...

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Autores principales: Lee, Ji Yeon, Hyun, Miri, Kim, Hyun Ah, Ryu, Seong Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992571/
https://www.ncbi.nlm.nih.gov/pubmed/33911650
http://dx.doi.org/10.5021/ad.2019.31.5.563
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author Lee, Ji Yeon
Hyun, Miri
Kim, Hyun Ah
Ryu, Seong Yeol
author_facet Lee, Ji Yeon
Hyun, Miri
Kim, Hyun Ah
Ryu, Seong Yeol
author_sort Lee, Ji Yeon
collection PubMed
description The Alternaria species are dematiaceous fungi. Human infection due to dematiaceous fungi is uncommon. Most reported cases of alternariosis have occurred in patients with immunodeficiency. The majority of cases were solid-organ transplantation recipients. Cutaneous alternariosis lesions are usually asymptomatic solitary nodules, plaques of ulcers or subcutaneous cysts. Here we report a case of a 77-year-old female who presented with hemorrhagic skin necrosis in right arm that had developed from hemorrhagic bullae. Her prior medical history included iatrogenic Cushing's syndrome, hypertension, interstitial lung disease and congestive heart failure. Following administration of itraconazole, her lesions improved.
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spelling pubmed-79925712021-04-27 Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate Lee, Ji Yeon Hyun, Miri Kim, Hyun Ah Ryu, Seong Yeol Ann Dermatol Case Report The Alternaria species are dematiaceous fungi. Human infection due to dematiaceous fungi is uncommon. Most reported cases of alternariosis have occurred in patients with immunodeficiency. The majority of cases were solid-organ transplantation recipients. Cutaneous alternariosis lesions are usually asymptomatic solitary nodules, plaques of ulcers or subcutaneous cysts. Here we report a case of a 77-year-old female who presented with hemorrhagic skin necrosis in right arm that had developed from hemorrhagic bullae. Her prior medical history included iatrogenic Cushing's syndrome, hypertension, interstitial lung disease and congestive heart failure. Following administration of itraconazole, her lesions improved. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019-10 2019-08-30 /pmc/articles/PMC7992571/ /pubmed/33911650 http://dx.doi.org/10.5021/ad.2019.31.5.563 Text en Copyright © 2019 The Korean Dermatological Association and The Korean Society for Investigative Dermatology 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 unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lee, Ji Yeon
Hyun, Miri
Kim, Hyun Ah
Ryu, Seong Yeol
Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate
title Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate
title_full Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate
title_fullStr Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate
title_full_unstemmed Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate
title_short Unusual Presentation of Subcutaneous Phaeohyphomycosis by Alternaria alternate
title_sort unusual presentation of subcutaneous phaeohyphomycosis by alternaria alternate
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992571/
https://www.ncbi.nlm.nih.gov/pubmed/33911650
http://dx.doi.org/10.5021/ad.2019.31.5.563
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