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Published on: September 20, 2018
Acute systemic histoplasmosis associated with chorioretinitis in an immunocompetent adolescent
Brian Fowler1, Christopher Shen, Joseph Mastellone
1Department of Ophthalmology, Hamilton Eye Institute, Memphis Medical Center, Memphis, Tennessee.
Abstract:
Histoplasmosis is an endemic, systemic mycosis caused by the dimorphic fungus Histoplasma capsulatum. A minority of patients develop asymptomatic chorioretinitis known as presumed ocular histoplasmosis syndrome (POHS), which is typically associated with chorioretinal scarring and peripapillary atrophy and occasionally with choroidal neovascularization secondary to maculopathy. We report a case of acute severe bilateral chorioretinitis associated with disseminated H. capsulatum in an immunocompetent adolescent boy living in an endemic area. The chorioretinitis did not respond to systemic antifungal therapy, but both his systemic illness and ocular lesions resolved with the addition of systemic steroids.
Insights
Severe ocular histoplasmosis in an adolescent boy resolved with steroids, not antifungals. This case highlights a unique treatment response for presumed ocular histoplasmosis syndrome (POHS) caused by Histoplasma capsulatum.
Area of Science:
- Ophthalmology
- Infectious Diseases
- Mycology
Background:
- Histoplasmosis, a systemic fungal infection caused by Histoplasma capsulatum, is endemic in certain regions.
- Presumed ocular histoplasmosis syndrome (POHS) is a manifestation of histoplasmosis, typically asymptomatic, causing chorioretinal scarring.
- Ocular complications like choroidal neovascularization can occur in POPS, impacting vision.
Purpose of the Study:
- To report a rare case of acute, severe bilateral chorioretinitis.
- To describe the association with disseminated Histoplasma capsulatum infection in an immunocompetent adolescent.
- To illustrate an unusual treatment response in a case of presumed ocular histoplasmosis syndrome (POHS).
Main Methods:
- Case report of an immunocompetent adolescent with disseminated Histoplasma capsulatum.
- Clinical presentation of acute severe bilateral chorioretinitis.
- Evaluation of treatment response to systemic antifungal therapy and subsequent addition of systemic steroids.
Main Results:
- The patient presented with acute, severe bilateral chorioretinitis.
- Initial systemic antifungal therapy was ineffective in resolving the ocular lesions.
- The addition of systemic steroids led to the resolution of both systemic illness and ocular manifestations.
Conclusions:
- Disseminated Histoplasma capsulatum can cause severe chorioretinitis in immunocompetent individuals.
- Presumed ocular histoplasmosis syndrome (POHS) may present acutely and severely.
- Systemic steroids can be effective in managing severe ocular histoplasmosis unresponsive to antifungals.
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