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. 75 No. 1, January 1966 TABLE OF CONTENTS
  Archives
  •  Online Features
  ARTICLES
 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
 •Citing articles on Web of Science (43)
 •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?

Amyloidosis of the Eyelid and Conjunctiva

MORTON E. SMITH, MD; LORENZ E. ZIMMERMAN, MD

Arch Ophthalmol. 1966;75(1):42-51.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Amyloidosis may be considered a group of disorders of diverse etiology and pathogenesis that have in common certain characteristic histopathologic features. Their essential unifying characteristic is the deposition in various tissues of a hyaline substance that can be distinguished from other types of hyalin by use of appropriate histopathologic technics. The exact nature of amyloid remains to be determined, however, and, in fact, there is reason for believing that amyloid deposits vary in composition sufficiently to form a spectrum from typical amyloid to nonspecific hyalin. The term "paramyloid" has been introduced to designate hyaline deposits that give atypical or inconsistent staining reactions for amyloid.

Several recent publications1-6 have reviewed the various concepts of the nature and pathogenesis of amyloidosis, but the clinicopathologic classification offered by Reimann and co-workers7 30 years ago continues to enjoy general acceptance:

  1. Primary amyloidosis, in which there is no known predisposing disease, characterized
. . . [Full Text PDF of this Article]


Author Affiliations

Washington, DC

From the Registry of Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, DC 20305.; Work was done during tenure of a Special Fellowship in Ophthalmic Pathology of the National Institute of Neurological Diseases and Blindness, NIH, at the Armed Forces Institute of Pathology (Dr. Smith). Present address: Department of Ophthalmology Washington University School of Medicine, St. Louis, Mo 63110. Chief, Ophthalmic Pathology Branch, Armed Forces Institute of Pathology (Dr. Zimmerman).


Footnotes

Submitted for publication May 10, 1965.

Reprint requests to Armed Forces Institute of Pathology, Washington, DC 20305.



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?





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1966 American Medical Association. All Rights Reserved.