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Volume 110, Issue 8, Pages 1626-1631 (August 2003)


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Late corneal perforation after photorefractive keratectomy associated with topical diclofenac: Involvement of matrix metalloproteinases

Presented at the meeting of the Association for Research in Vision and Ophthalmology, Ft. Lauderdale, Florida, May 2002.

Eric E Gabison, MD12, Philippe Chastang, MD1, Suzanne Menashi, PhD2, Samia Mourah, PharmD3, Serge Doan, MD1, Michelle Oster2, Alain Mauviel, PhD2, Thanh Hoang-Xuan, MD1Corresponding Author Information

Received 16 September 2002; accepted 14 February 2003.

Abstract 

Objective

To report a case of a 50-year-old man who was initially seen with a corneal perforation in his right eye 2 months after a photorefractive keratectomy (PRK) procedure and to discuss the roles of topical diclofenac and matrix metalloproteinases (MMPs).

Design

Case report with tissue analysis.

Main outcome measures

Ocular examination, diagnostic workup, surgical treatment, and histologic, immunofluorescent, zymography, and real time-polymerase chain reaction studies on corneal button.

Results

Slit-lamp examination of the right eye revealed a 4-mm diameter area of central corneal thinning with a 2-mm diameter perforation at its center. Predisposing factors included prolonged postoperative topical diclofenac therapy for more than 2 months and a 10-year history of well-controlled diabetes mellitus. An extensive diagnostic workup ruled out a systemic autoimmune disease. A penetrating keratoplasty was performed. Results of immunohistochemical studies of the corneal button showed stromal accumulation of temporary type III and IV collagens, MMP-3, and MMP-9 in the anterior wounded stroma and MMP-9 in the basal corneal epithelial cells of the leading edge. Differential activity and expression of MMP-2 and MMP-9 were found between the central and peripheral corneal buttons.

Conclusions

Prolonged use of diclofenac and diabetes mellitus might be responsible for the corneal perforation after PRK in our patient. MMP-9 and MMP-3 might be involved in delayed wound closure and corneal melting.

1 Fondation Ophtalmologique A. de Rothschild, Paris, France

2 INSERM U532, Institut de Recherche sur la Peau, Hôpital St. Louis, Paris, France

3 Institut de Génétique Moléculaire, Hôpital St. Louis, Paris, France

Corresponding Author InformationReprint requests to Professeur Thanh Hoang-Xuan, Fondation Ophtalmologique A. de Rothschild, 25-29 rue Manin, 75940 Paris Cedex 19, France.

 Manuscript no. 220731.

Supported by the Association Française des Amblyopes Unilatéraux, Paris, France.

None of the authors has any commercial interest that could cause or be perceived to be a conflict of interest.

PII: S0161-6420(03)00486-X

doi:10.1016/S0161-6420(03)00486-X


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