rss
Br J Ophthalmol 1997;81:1 doi:10.1136/bjo.81.1.1
  • Editorial

Presumed ocular histoplasmosis syndrome in the Netherlands

  1. GERALD J ROPER,
  2. HENRY J KAPLAN
  1. Department of Ophthalmology and Visual Sciences
  2. Washington University School of Medicine
  3. 660 South Euclid Avenue, St Louis, MO 93110, USA

      The presumed ocular histoplasmosis syndrome (POHS) occurs in areas of the USA in which Histoplasma capsulatumis endemic. The ocular triad of POHS consists of peripheral punched out chorioretinal scars, peripapillary atrophy, and maculopathy. The maculopathy most frequently consists of a subretinal neovascular complex associated with a previous focal chorioretinal scar. Vitritis is not observed in POHS.

      The characteristic ocular presentation was associated with infection with H capsulatum through epidemiological studies.12 However, only rarely has the H capsulatum antigen and organism been identified in an eye with POHS. Khalil enucleated an eye with choroidal melanoma and demonstrated chorioretinal foci with various stages of chronic inflammation in which both the antigen …

      This Article

      Services

      1. Request permissions

      Responses

      1. Submit a response
      2. No responses published

      Social bookmarking

      Register for free content


      Free sample
      This recent issue is free to all users to allow everyone the opportunity to see the full scope and typical content of BJO.
      View free sample issue >>

      Free archive
      The full back archive is now available for BJO. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006, back to volume 1 issue 1.
      Register to access the free archive >>

      Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.