Presumed Ocular Histoplasmosis Syndrome (POHS) can silently impact your retinal health. It’s crucial to understand the risks and symptoms, and our expert specialists are here to guide you on maintaining optimal vision. Find a top optometrist near you now for a thorough evaluation.
This page provides detailed information on Presumed Ocular Histoplasmosis Syndrome (POHS), covering its overview, causes, diagnosis, treatment options, long-term management, and essential guidance for maintaining vision.
Presumed Ocular Histoplasmosis Syndrome (POHS) is an eye condition that impacts the retina, the light-sensitive layer at the back of your eye, and may affect your vision. It is linked to past exposure to a common soil fungus, Histoplasma capsulatum, which is found in areas like the Ohio and Mississippi River valleys. Recognizing POHS early is important because, although many people may never notice symptoms, timely monitoring can help prevent vision loss if abnormal blood vessel growth develops.
POHS is a condition where small, often silent scars known as histo spots form on the retina from previous exposure to the Histoplasma fungus. These scars are a result of what is believed to be an immune response after inhaling fungal spores; most individuals come into contact with this fungus without experiencing any eye-related issues. In some cases, however, these scars trigger the growth of abnormal blood vessels in the retina, a process called choroidal neovascularization (CNV), which can lead to vision problems.
Here’s the thing, POHS usually does not present noticeable symptoms in its early stages. The retina may look normal to the naked eye until abnormal blood vessels begin to develop near the central vision area, known as the macula. When this happens, you might experience changes in vision that require prompt attention to ensure the best possible outcomes.
When complications arise due to POHS, you could notice certain visual disturbances that signal a change in your eye health. These symptoms may develop either gradually or suddenly, and even subtle changes are worth noting. If you start noticing any unusual changes in your vision, it’s best to seek guidance from our retina specialists immediately. Watch out for:
The exact pathway that leads from exposure to Histoplasma capsulatum to POHS is still being researched. However, experts believe that the process begins when you inhale fungal spores, usually in regions where the fungus thrives in soil enriched with bird or bat droppings. For most people, this exposure results in a mild or unnoticed lung infection, but in some cases, the fungus appears to trigger small scars in the retina later on.
These retinal scars or “histo spots” do not cause problems by themselves but can later foster the development of abnormal blood vessels around the retina. This growth, termed choroidal neovascularization, disrupts the normal structure and function of the retina, leading to potential vision loss if left untreated.
Although many people are exposed to Histoplasma capsulatum at some point in life, only a handful develop POHS. Factors that may increase one’s risk include:
Regular eye exams are key to detecting POHS early, even when symptoms have not yet appeared. During a comprehensive evaluation, our retina specialists focus on examining the retina for the telltale signs of POHS, including histo spots, abnormal blood vessel growth, or other subtle changes.
The diagnosis involves a step-by-step process with imaging tests that provide a closer look into the retina:
Anti-VEGF therapy is considered the frontline treatment for vision loss associated with POHS. The medication works by blocking vascular endothelial growth factor, a substance that encourages the growth of abnormal blood vessels. The treatment is often administered on a monthly basis initially. As your eye responds, the frequency may be adjusted. Many patients experience stabilization of their vision, and in some cases, improvements have been noted when treatment is initiated early. Here’s what typically happens during this treatment:
Before anti-VEGF injections became widely available, laser photocoagulation was a common treatment option. This procedure uses a laser to seal off leaking blood vessels in the retina. However, due to the risk of creating permanent blind spots, laser therapy is now reserved for specific cases where abnormal blood vessels are not directly affecting the center of vision.
Don’t wait for symptoms to develop! Contact our experienced retina specialists today to schedule a comprehensive eye exam and discuss any concerns you might have about Presumed Ocular Histoplasmosis Syndrome. Your vision deserves attentive care!
In addition to these procedures, some patients may benefit from photodynamic therapy (PDT). With PDT, a light-sensitive drug is introduced into your bloodstream, accumulating in the abnormal vessels. A low-power laser then activates this medication to help close off the problematic blood vessels. While PDT is less common now, it remains an option in scenarios where anti-VEGF therapy may not be fully effective.
Even if you are not presently experiencing symptoms, regular monitoring is essential when you have a history of histoplasmosis or other risk factors associated with POHS. Our retina specialists emphasize the importance of keeping a close watch on your vision, as changes can occur suddenly.
While the prospect of POHS can be concerning, it is important to remember that many individuals maintain good vision with early detection and appropriate treatment. Understanding your condition and being proactive in scheduling regular eye exams can help you feel more in control of your eye health. The commitment of our retina specialists is to work with you every step of the way, ensuring that you receive personalized care tailored to your needs.
Your treatment plan is designed to minimize vision loss and maintain the quality of your sight, offering hope and improved outcomes even when facing complications from this condition.
Since POHS requires lifelong monitoring, staying informed and vigilant about your eye health is essential. It is reassuring to know that modern treatments and refined diagnostic tools have significantly improved how we manage this condition, allowing many patients to enjoy a good quality of vision over the long term.
No, POHS is not an active infection. It is a condition that results from a past exposure to Histoplasma capsulatum. The fungus itself is not actively infecting the eye; instead, it is the scarring from the previous exposure that may eventually lead to complications in vision.
In most cases, exposure to Histoplasma capsulatum does not result in POHS. Many people inhale the fungal spores during their lifetime without ever experiencing symptoms or changes in their eye health. POHS tends to develop only in a small percentage of individuals who have a certain predisposition or additional risk factors.
Vision changes related to POHS can occur either gradually or suddenly, particularly if choroidal neovascularization develops. While many patients do not notice any changes initially, any sudden appearance of blurred or distorted vision should be addressed immediately by our retina specialists for a thorough evaluation.
Since Histoplasma capsulatum is present in the environment, it is difficult to avoid exposure completely. However, if you know that you are at risk, especially if you live in high-prevalence areas, it is important to be mindful of activities that may stir up contaminated soil, such as working near chicken coops or in areas with bat droppings. Regular eye examinations are the best way to catch any early signs of POHS before they affect your vision.
Don’t wait for symptoms to develop! Contact our experienced retina specialists today to schedule a comprehensive eye exam and discuss any concerns you might have about Presumed Ocular Histoplasmosis Syndrome. Your vision deserves attentive care!
Get insight into Presumed Ocular Histoplasmosis Syndrome (POHS), exploring causes, symptoms, diagnosis, and treatment options for maintaining eye health.
