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Published Online First: 6 December 2006. doi:10.1136/bjo.2006.107243
British Journal of Ophthalmology 2007;91:588-591
Copyright © 2007 by the BMJ Publishing Group Ltd.

SCIENTIFIC REPORT

In vivo confocal microscopy in fungal keratitis

Emmanuelle Brasnu1, Tristan Bourcier2, Bénédicte Dupas1, Sandrine Degorge3, Thibault Rodallec4, Laurent Laroche5, Vincent Borderie5 and Christophe Baudouin6

1 Department of Ophthalmology III, Quinze-Vingts National Center of Ophthalmology, Paris, France
2 Department of Ophthalmology, Strasbourg Universitary Hospital, Strasbourg, France
3 Quinze-Vingts National Center of Ophthalmology, Laboratory, Paris, France
4 Department of Ophthalmology II, Quinze-Vingts National Center of Ophthalmology, Paris, France
5 Department of Ophthalmology V, Quinze-Vingts National Center of Ophthalmology, Paris, France
6 Quinze-Vingts National Center of Ophthalmology, Department of Ophthalmology III, Paris, France; INSERM, UMR S 872, Cordeliers Biomedical Institute, Paris Descartes and Pierre et Marie Curie Universities, Paris, France

Correspondence to:
Correspondence to:
Professor C Baudouin
Hôpital des Quinze-Vingts, Service III, 28 rue de Charenton, 75012 Paris, France; baudouin{at}quinze-vingts.fr

ABSTRACT

Background: Fungal keratitis is a major blinding eye disease found throughout the world, particularly in developing countries. Given the recent increase in Fusarium keratitis infections in contact lens wearers owing to contact lens solutions, a warning was recently issued by the Food and Drug Administration, making it a public health concern in developed countries.

Objective: To show the advantages of in vivo confocal microscopy imaging using the Heidelberg Retina Tomograph II-Rostock Cornea Module (HRTII-RCM) in the early diagnosis of fungal keratitis.

Methods: HRTII-RCM confocal microscopy was performed on five patients presenting with fungal keratitis and on three donor corneas contaminated with Fusarium solani, Aspergillus fumigatus and Candida albicans.

Results: Direct microscopic evaluation of corneal smears and culture revealed the presence of F solani in four cases and C albicans in one case. HRTII-RCM examination of the infected patients and contaminated donor corneas revealed numerous high-contrast elements resembling Fusarium, Aspergillus hyphae or Candida pseudofilaments in the anterior stroma.

Conclusion: HRTII-RCM in vivo confocal microscopy is a new, non-invasive and rapid technique for the early diagnosis of fungal keratitis, showing high-resolution images resembling fungal structures in the early phase of the disease.

Abbreviations: FK, fungal keratitis; HRTII-RCM, Heidelberg Retina Tomograph II-Rostock Cornea Module


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