Paraneoplastic uveitis

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:279928H57.8
Who is this for?
Show terms as
1FDA treatments1Specialists8Treatment centers

Where are you in your journey?

UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
Report missing data

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.

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

FDA & Trial Timeline

1 event
Apr 1999

DepoCyt: FDA approved

Intrathecal treatment of lymphomatous meningitis.

FDAcompleted

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

1 available

DepoCyt

Cytarabine liposomal· Pacira Pharmaceuticals, Inc.Orphan Drug

Intrathecal treatment of lymphomatous meningitis.

No actively recruiting trials found for Paraneoplastic uveitis at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Paraneoplastic uveitis community →

Specialists

1 foundView all specialists →

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Paraneoplastic uveitis.

Search all travel grants →NORD Financial Assistance ↗

Community

Open Paraneoplastic uveitisForum →

No community posts yet. Be the first to share your experience with Paraneoplastic uveitis.

Start the conversation →

Latest news about Paraneoplastic uveitis

No recent news articles for Paraneoplastic uveitis.

Follow this condition to be notified when news becomes available.

Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

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.