You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 113 No. 3, March 1995 TABLE OF CONTENTS
  Archives
  •  Online Features
  Clinicopathologic Reports
 This Article
 •References
 •Full text PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Immunohistochemical Analysis of the Pathogenesis of Posterior Polymorphous Dystrophy

Joel R. Ross, PhD; Gary N. Foulks, MD; Fred P. Sanfilippo, MD, PhD; David N. Howell, MD, PhD

Arch Ophthalmol. 1995;113(3):340-345.


Abstract

The pathogenesis of posterior polymorphous dystrophy was analyzed by immunohistologic methods. Sections of corneal buttons from two patients undergoing transplantation owing to posterior polymorphous dystrophy were stained with 2B4.14.1, a monoclonal antibody that reacts with human corneal endothelium, and with a cocktail of antihuman cytokeratin monoclonal antibodies that do not react with normal corneal endothelium. Single-stained sections revealed a variegated, intermittent staining pattern of antibody reactive and nonreactive cells. Double-stained sections revealed some cells that stained with only one of the antibodies and many cells that stained with both antibodies. The presence of cells staining positively for both 2B4.14.1 antigen and cytokeratins supports the hypothesis that the cytokeratin-expressing epithelial-like cells found in corneas with posterior polymorphous dystrophy arise via a metaplastic process in which the phenotype of endothelial cells becomes progressively abnormal.



Author Affiliations

From the Departments of Ophthalmology (Drs Ross and Foulks) and Pathology (Dr Howell), Durham (NC) Veterans Affairs Medical Center and Duke University Medical Center, Durham; and the Department of Pathology, The Johns Hopkins School of Medicine, Baltimore, Md (Dr Sanfilippo).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Missense mutations in COL8A2, the gene encoding the {alpha}2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
Biswas et al.
Hum Mol Genet 2001;10:2415-2423.
ABSTRACT | FULL TEXT  

Ultrasound biomicroscopic images of the anterior chamber angle of a patient with posterior polymorphous dystrophy
KATAI et al.
Br J Ophthalmol 1998;82:1339-1339.
FULL TEXT  

Early-Onset Posterior Polymorphous Dystrophy
Levy et al.
Arch Ophthalmol 1996;114:1265-1268.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1995 American Medical Association. All Rights Reserved.