Cargando…
Infectious endotheliitis: a rare case of presumed mycotic origin
PURPOSE: To report an interesting case of infectious endotheliitis of presumed mycotic origin. METHODS: A case report of a 56-year-old male farmer who sought medical attention after a month-long evolution of irritative symptoms in his right eye, accompanied by visual acuity (VA) impairment. The pati...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720662/ https://www.ncbi.nlm.nih.gov/pubmed/23901253 http://dx.doi.org/10.2147/OPTH.S43695 |
_version_ | 1782277982044291072 |
---|---|
author | Zapata, Luis Fernando Paulo, José David Restrepo, Carlos A Velásquez, Luis Fernando Montoya, Andrés E Toro Zapata, Melissa A |
author_facet | Zapata, Luis Fernando Paulo, José David Restrepo, Carlos A Velásquez, Luis Fernando Montoya, Andrés E Toro Zapata, Melissa A |
author_sort | Zapata, Luis Fernando |
collection | PubMed |
description | PURPOSE: To report an interesting case of infectious endotheliitis of presumed mycotic origin. METHODS: A case report of a 56-year-old male farmer who sought medical attention after a month-long evolution of irritative symptoms in his right eye, accompanied by visual acuity (VA) impairment. The patient received topical and oral broad-spectrum antibiotic treatment with no improvement before being referred to a cornea specialist, where he was found to have VA of 20/150 and was noted on biomicroscopy to have endothelial feathery coalescent lesions. The patient was admitted to the hospital for an aqueous humor sample and intravenous voriconazole. RESULTS: The microbiological studies did not isolate any micro-organisms. However, clinical evidence of improvement was confirmed after 5 days of antimycotic intravenous therapy. Complete clinical resolution was achieved at 1 month after treatment completion with oral voriconazole, as evidenced by VA of 20/20 and disappearance of endothelial lesions. CONCLUSION: Endothelial involvement by fungi is a rare condition. In this case, no microbes were isolated, but the characteristic morphology of the lesions, the history of onychomycosis, and the spectacular response to voriconazole turn this case into a valid presumptive diagnosis. |
format | Online Article Text |
id | pubmed-3720662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37206622013-07-30 Infectious endotheliitis: a rare case of presumed mycotic origin Zapata, Luis Fernando Paulo, José David Restrepo, Carlos A Velásquez, Luis Fernando Montoya, Andrés E Toro Zapata, Melissa A Clin Ophthalmol Case Report PURPOSE: To report an interesting case of infectious endotheliitis of presumed mycotic origin. METHODS: A case report of a 56-year-old male farmer who sought medical attention after a month-long evolution of irritative symptoms in his right eye, accompanied by visual acuity (VA) impairment. The patient received topical and oral broad-spectrum antibiotic treatment with no improvement before being referred to a cornea specialist, where he was found to have VA of 20/150 and was noted on biomicroscopy to have endothelial feathery coalescent lesions. The patient was admitted to the hospital for an aqueous humor sample and intravenous voriconazole. RESULTS: The microbiological studies did not isolate any micro-organisms. However, clinical evidence of improvement was confirmed after 5 days of antimycotic intravenous therapy. Complete clinical resolution was achieved at 1 month after treatment completion with oral voriconazole, as evidenced by VA of 20/20 and disappearance of endothelial lesions. CONCLUSION: Endothelial involvement by fungi is a rare condition. In this case, no microbes were isolated, but the characteristic morphology of the lesions, the history of onychomycosis, and the spectacular response to voriconazole turn this case into a valid presumptive diagnosis. Dove Medical Press 2013 2013-07-18 /pmc/articles/PMC3720662/ /pubmed/23901253 http://dx.doi.org/10.2147/OPTH.S43695 Text en © 2013 Zapata et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Case Report Zapata, Luis Fernando Paulo, José David Restrepo, Carlos A Velásquez, Luis Fernando Montoya, Andrés E Toro Zapata, Melissa A Infectious endotheliitis: a rare case of presumed mycotic origin |
title | Infectious endotheliitis: a rare case of presumed mycotic origin |
title_full | Infectious endotheliitis: a rare case of presumed mycotic origin |
title_fullStr | Infectious endotheliitis: a rare case of presumed mycotic origin |
title_full_unstemmed | Infectious endotheliitis: a rare case of presumed mycotic origin |
title_short | Infectious endotheliitis: a rare case of presumed mycotic origin |
title_sort | infectious endotheliitis: a rare case of presumed mycotic origin |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720662/ https://www.ncbi.nlm.nih.gov/pubmed/23901253 http://dx.doi.org/10.2147/OPTH.S43695 |
work_keys_str_mv | AT zapataluisfernando infectiousendotheliitisararecaseofpresumedmycoticorigin AT paulojosedavid infectiousendotheliitisararecaseofpresumedmycoticorigin AT restrepocarlosa infectiousendotheliitisararecaseofpresumedmycoticorigin AT velasquezluisfernando infectiousendotheliitisararecaseofpresumedmycoticorigin AT montoyaandresetoro infectiousendotheliitisararecaseofpresumedmycoticorigin AT zapatamelissaa infectiousendotheliitisararecaseofpresumedmycoticorigin |