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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...

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Autores principales: Zapata, Luis Fernando, Paulo, José David, Restrepo, Carlos A, Velásquez, Luis Fernando, Montoya, Andrés E Toro, Zapata, Melissa A
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
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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.
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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
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