Infectious endotheliitis: a rare case of presumed mycotic origin

Luis Fernando Zapata,1 José David Paulo,1 Carlos A Restrepo,1 Luis Fernando Velásquez,2 Andrés E Toro Montoya,2 Melissa A Zapata21Department of Ophthalmology Hospital Pablo Tobón Uribe; 2School of Medicine, Universidad Pontificia Bolivariana, Medell&ia...

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Main Authors: Zapata LF, Paulo JD, Restrepo CA, Velásquez LF, Toro Montoya AE, Zapata MA
Format: Article
Language:English
Published: Dove Medical Press 2013-07-01
Series:Clinical Ophthalmology
Online Access:http://www.dovepress.com/infectious-endotheliitis-a-rare-case-of-presumed-mycotic-origin-a13697
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spelling doaj-2f49dde375f7433e95382240327bccf82020-11-24T23:30:21ZengDove Medical PressClinical Ophthalmology1177-54671177-54832013-07-012013default14591461Infectious endotheliitis: a rare case of presumed mycotic originZapata LFPaulo JDRestrepo CAVelásquez LFToro Montoya AEZapata MALuis Fernando Zapata,1 José David Paulo,1 Carlos A Restrepo,1 Luis Fernando Velásquez,2 Andrés E Toro Montoya,2 Melissa A Zapata21Department of Ophthalmology Hospital Pablo Tobón Uribe; 2School of Medicine, Universidad Pontificia Bolivariana, Medellín, ColombiaPurpose: 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.Keywords: endotheliitis, mycotic, keratitis, voriconazolehttp://www.dovepress.com/infectious-endotheliitis-a-rare-case-of-presumed-mycotic-origin-a13697
collection DOAJ
language English
format Article
sources DOAJ
author Zapata LF
Paulo JD
Restrepo CA
Velásquez LF
Toro Montoya AE
Zapata MA
spellingShingle Zapata LF
Paulo JD
Restrepo CA
Velásquez LF
Toro Montoya AE
Zapata MA
Infectious endotheliitis: a rare case of presumed mycotic origin
Clinical Ophthalmology
author_facet Zapata LF
Paulo JD
Restrepo CA
Velásquez LF
Toro Montoya AE
Zapata MA
author_sort Zapata LF
title Infectious endotheliitis: a rare case of presumed mycotic origin
title_short 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_sort infectious endotheliitis: a rare case of presumed mycotic origin
publisher Dove Medical Press
series Clinical Ophthalmology
issn 1177-5467
1177-5483
publishDate 2013-07-01
description Luis Fernando Zapata,1 José David Paulo,1 Carlos A Restrepo,1 Luis Fernando Velásquez,2 Andrés E Toro Montoya,2 Melissa A Zapata21Department of Ophthalmology Hospital Pablo Tobón Uribe; 2School of Medicine, Universidad Pontificia Bolivariana, Medellín, ColombiaPurpose: 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.Keywords: endotheliitis, mycotic, keratitis, voriconazole
url http://www.dovepress.com/infectious-endotheliitis-a-rare-case-of-presumed-mycotic-origin-a13697
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