Presumed ocular histoplasmosis syndrome

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Presumed ocular histoplasmosis syndrome
Presumed ocular histoplasmosis syndrome
Synonyms	POHS
Pronounce	N/A
Specialty	N/A
Symptoms	Chorioretinitis, vision loss, scotoma
Complications	Choroidal neovascularization, retinal detachment
Onset	Typically in adulthood
Duration	Chronic
Types	N/A
Causes	Presumed to be related to Histoplasma capsulatum infection
Risks	Living in areas endemic to Histoplasmosis
Diagnosis	Clinical examination, fluorescein angiography, optical coherence tomography
Differential diagnosis	Age-related macular degeneration, toxoplasmosis, sarcoidosis
Prevention	N/A
Treatment	Anti-VEGF therapy, laser photocoagulation, corticosteroids
Medication	N/A
Prognosis	Variable, depends on extent of choroidal neovascularization
Frequency	More common in Ohio River Valley and Mississippi River Valley
Deaths	N/A

Presumed Ocular Histoplasmosis Syndrome (POHS) is a rare eye disease that is believed to be caused by the Histoplasma capsulatum fungus. This condition is characterized by the presence of chorioretinal scars, peripapillary atrophy, and choroidal neovascularization in the absence of systemic histoplasmosis or evidence of other causes of similar ocular findings.

Etiology

The exact cause of POHS is not well understood. It is presumed to be caused by the Histoplasma capsulatum fungus, which is endemic in certain parts of the United States, particularly the Ohio River Valley and the Mississippi River Valley. However, not all individuals exposed to the fungus develop POHS, suggesting that other factors, possibly genetic, may also play a role.

Clinical Presentation

Patients with POHS typically present with symptoms of blurred vision, scotoma (blind spot), and sometimes metamorphopsia (distorted vision). On ophthalmic examination, characteristic findings include small, round, punched-out chorioretinal scars known as "histo spots," peripapillary atrophy, and choroidal neovascularization.

Diagnosis

The diagnosis of POHS is primarily clinical, based on the characteristic ocular findings in the absence of systemic histoplasmosis or other causes of similar ocular findings. Fluorescein angiography and optical coherence tomography (OCT) may be used to confirm the diagnosis and assess the extent of choroidal neovascularization.

Treatment

The primary treatment for POHS is aimed at controlling the choroidal neovascularization, which can lead to severe vision loss if left untreated. This is typically achieved with intravitreal injections of anti-vascular endothelial growth factor (anti-VEGF) agents. Laser photocoagulation may also be used in some cases.

Prognosis

The prognosis for POHS varies depending on the extent of choroidal neovascularization and the response to treatment. With early detection and treatment, vision loss can often be prevented or minimized.

See Also

• Histoplasmosis
• Choroidal neovascularization
• Ocular diseases

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