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Article
May 1964

Meesmann's Corneal DystrophyA Pathological Study

Author Affiliations

Boston
Howe Laboratory of Ophthalmology, Harvard University Medical School, and Massachusetts Eye and Ear Infirmary.

Arch Ophthalmol. 1964;71(5):676-682. doi:10.1001/archopht.1964.00970010692015
Abstract

A rare form of familial dystrophy of the corneal epithelium was described clinically by Pameijer1 in 1935. In 1938 Meesmann2 studied this dystrophy pathologically and found an abundance of glycogen in the corneal epithelium. Although other authors have described this dystrophy,3-6 none has identified conclusively as glycogen the deposits which Meesmann reported.

The purpose of this communication is to report a case with histochemical and finestructural studies and to suggest a possible pathogenesis of the disease.

Report of Case  The propositus was a 31-year-old white female, who was first seen in the clinic of the Massachusetts Eye and Ear Infirmary in September, 1961. She had been sent on referral for diagnosis of "black spots" of unknown duration in the cornea. Her only subjective complaint was occasional ocular irritation.Vision with correction for myopic astigmatism in each eye was 20/40-2 OD and 20/60 OS. The corneas were studded

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