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Presumed ocular histoplasmosis syndrome (POHS)

< 1 min read

Presumed ocular histoplasmosis syndrome POHS is a retinal condition linked to previous infection with the fungus Histoplasma capsulatum. It can cause sight-threatening choroidal neovascularisation near the macula.

Features and symptoms

Most people with POHS have no active infection, only old scars. Vision changes occur if new vessels form.

  • Punched-out atrophic scars in the mid-periphery and around the optic disc
  • Absence of significant vitreous inflammation
  • Distortion or central blur when choroidal neovascular membranes develop
  • More common in people from histoplasmosis-endemic regions

Treatment

Management focuses on treating any choroidal neovascularisation and monitoring the fellow eye.

  • Intravitreal anti-VEGF injections for active neovascular membranes
  • OCT and angiography to guide treatment and follow-up
  • Self-monitoring with an Amsler grid to detect new distortion
  • Low-vision support if central scarring is advanced