Overview
Paraneoplastic uveitis is a rare inflammatory condition of the uveal tract (the middle vascular layer of the eye, comprising the iris, ciliary body, and choroid) that occurs as a paraneoplastic phenomenon — meaning it arises not from direct tumor invasion of the eye, but as an immune-mediated response triggered by a distant malignancy. The condition is classified among paraneoplastic ocular syndromes and may be associated with various underlying cancers, including lymphomas, lung carcinomas, and other solid or hematologic malignancies. The immune system, activated against tumor antigens, cross-reacts with normal ocular tissues, leading to intraocular inflammation. Patients typically present with eye redness, pain, photophobia (light sensitivity), blurred vision, and floaters. The uveitis may be anterior (affecting the iris and ciliary body), intermediate, posterior (affecting the choroid and retina), or panuveitic. It can be unilateral or bilateral. Because the ocular symptoms may precede the diagnosis of the underlying malignancy, recognition of the paraneoplastic nature of the uveitis is critical for early cancer detection. Other paraneoplastic ocular conditions, such as cancer-associated retinopathy (CAR) and melanoma-associated retinopathy (MAR), may overlap or coexist. Treatment of paraneoplastic uveitis involves a dual approach: management of the underlying malignancy and control of the ocular inflammation. Topical and systemic corticosteroids are commonly used to reduce intraocular inflammation. Immunosuppressive agents may be required in refractory cases. Successful treatment of the underlying cancer often leads to improvement or resolution of the uveitis. Prognosis depends on the nature and stage of the associated malignancy as well as the severity and chronicity of the ocular inflammation. Early referral to both an oncologist and an ophthalmologist experienced in uveitis is essential for optimal outcomes.
Adult
Begins in adulthood (age 18 or older)
FDA & Trial Timeline
1 eventDepoCyt: FDA approved
Intrathecal treatment of lymphomatous meningitis.
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
1 availableDepoCyt
Intrathecal treatment of lymphomatous meningitis.
Clinical Trials
View all trials with filters →No actively recruiting trials found for Paraneoplastic uveitis at this time.
New trials open frequently. Follow this disease to get notified.
Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Paraneoplastic uveitis.
Community
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Caregiver Resources
NORD Caregiver Resources
Support, advocacy, and financial assistance for caregivers of rare disease patients.
Mental Health Support
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Family & Caregiver Grants
Financial assistance programs specifically for caregivers of rare disease patients.
Social Security Disability
Learn how rare disease patients may qualify for SSDI/SSI benefits.
Common questions about Paraneoplastic uveitis
What is Paraneoplastic uveitis?
Paraneoplastic uveitis is a rare inflammatory condition of the uveal tract (the middle vascular layer of the eye, comprising the iris, ciliary body, and choroid) that occurs as a paraneoplastic phenomenon — meaning it arises not from direct tumor invasion of the eye, but as an immune-mediated response triggered by a distant malignancy. The condition is classified among paraneoplastic ocular syndromes and may be associated with various underlying cancers, including lymphomas, lung carcinomas, and other solid or hematologic malignancies. The immune system, activated against tumor antigens, cross
At what age does Paraneoplastic uveitis typically begin?
Typical onset of Paraneoplastic uveitis is adult. Age of onset can vary across affected individuals.
Which specialists treat Paraneoplastic uveitis?
1 specialists and care centers treating Paraneoplastic uveitis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.
What treatment and support options exist for Paraneoplastic uveitis?
1 patient support program are currently tracked on UniteRare for Paraneoplastic uveitis. See the treatments and support programs sections for copay assistance, eligibility, and contact details.