May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
HETEROGENEITY OF KERATIC PRECIPITATES REVEALED BY IN VIVO CONFOCAL IMAGING. A NEW DIAGNOSTIC TOOL?
Author Affiliations & Notes
  • M.S. Wertheim
    Casey Eye Institute, Oregon Health & Science University, Portland, OR
  • W.D. Mathers
    Casey Eye Institute, Oregon Health & Science University, Portland, OR
  • J.R. Smith
    Casey Eye Institute, Oregon Health & Science University, Portland, OR
  • T.M. Martin
    Casey Eye Institute, Oregon Health & Science University, Portland, OR
  • S.R. Planck
    Casey Eye Institute, Oregon Health & Science University, Portland, OR
  • J.T. Rosenbaum
    Casey Eye Institute, Oregon Health & Science University, Portland, OR
  • Footnotes
    Commercial Relationships  M.S. Wertheim, None; W.D. Mathers, None; J.R. Smith, None; T.M. Martin, None; S.R. Planck, None; J.T. Rosenbaum, None.
  • Footnotes
    Support  National Eye Institute RO3–EY014013
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 2689. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      M.S. Wertheim, W.D. Mathers, J.R. Smith, T.M. Martin, S.R. Planck, J.T. Rosenbaum; HETEROGENEITY OF KERATIC PRECIPITATES REVEALED BY IN VIVO CONFOCAL IMAGING. A NEW DIAGNOSTIC TOOL? . Invest. Ophthalmol. Vis. Sci. 2004;45(13):2689.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Abstract: : Purpose: Formation of keratic precipitates (KP) is a characteristic finding in various forms of intraocular inflammation, including uveitis and corneal transplant rejection. Clinically KP may take a limited number of forms distinguished by size and distribution across the corneal endothelium. We evaluated the heterogeneity of KP in subtypes of uveitis by scanning confocal microscopy, a technique providing 500–fold magnification. Methods: Cornea and KP were viewed with an ASL–1000 Scanning Confocal Microscope (Advanced Scanning Ltd, New Orleans, LO) in patients (n=35) presenting to a tertiary referral uveitis service with immune–mediated and infectious forms of uveitis, including HLA B27–associated, sarcoidosis, Vogt–Koyanagi–Harada syndrome, juvenile idiopathic arthritis, Fuchs’ heterochromic iridocyclitis, CMV retinitis, herpetic anterior uveitis, ocular toxoplasmosis and idiopathic uveitis. Images were captured and digitalized in real time. Results: Keratic precipitates were successfully imaged by this non–invasive confocal microscopy system. Three–dimensional views were rendered from z–stacks of certain images. The KP could be classified into distinct morphological patterns including: smooth rounded, globular, dendritiform, cruciform and stellate. In general, in any given patient, the morphology of KP was consistent across the endothelium. Likewise, patients with a given disease tended to have KPs with similar morphologies. Patients with infections demonstrated KP architecture usually distinct from a non–infectious process. Conclusions: Scanning confocal microscopy has been used for the first time to describe the anatomy of KP in uveitis. Such observations reveal a heterogeneity that could not be appreciated by conventional slit lamp microscopy and may have diagnostic relevance.

Keywords: uveitis–clinical/animal model • imaging/image analysis: clinical 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×