Overview
Infectious scleritis is a rare and serious inflammatory condition of the sclera (the tough, white outer coat of the eye) caused by microbial organisms, including bacteria, fungi, viruses, or parasites. Unlike autoimmune or idiopathic scleritis, infectious scleritis results from direct invasion of the scleral tissue by pathogens. It most commonly occurs following ocular surgery (particularly pterygium surgery with adjunctive mitomycin C or beta-irradiation), ocular trauma, or extension of infection from adjacent structures such as the cornea. Rarely, it may arise from hematogenous spread of systemic infections. The condition primarily affects the eye but can lead to devastating complications including scleral necrosis, perforation, endophthalmitis, and permanent vision loss if not promptly diagnosed and treated. Key symptoms include severe, deep ocular pain that may worsen at night and with eye movement, localized or diffuse redness of the eye, tenderness, tearing, photophobia, and decreased visual acuity. A characteristic finding may include a scleral abscess or area of scleral necrosis with surrounding inflammation. The most commonly implicated organisms include Pseudomonas aeruginosa, Staphylococcus species, Streptococcus species, Nocardia, and various fungi such as Aspergillus and Fusarium species. Atypical mycobacteria and Acanthamoeba are also recognized causative agents. Diagnosis requires a high index of clinical suspicion, particularly in patients with a history of prior ocular surgery or trauma. Scleral biopsy or scraping with microbiological cultures and sensitivity testing is essential for identifying the causative organism and guiding targeted therapy. Treatment involves intensive, prolonged antimicrobial therapy tailored to the identified pathogen, which may include topical, subconjunctival, systemic, or intravitreal antibiotics or antifungals. Surgical debridement of necrotic scleral tissue may be necessary, and scleral patch grafting may be required in cases of significant tissue loss or perforation. Despite aggressive treatment, the prognosis can be guarded, and some patients may experience significant visual morbidity.
Adult
Begins in adulthood (age 18 or older)
FDA & Trial Timeline
1 eventImperial College London — NA
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
No FDA-approved treatments are currently listed for Infectious scleritis.
View clinical trials →Clinical Trials
View all trials with filters →No actively recruiting trials found for Infectious scleritis at this time.
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Rare Disease Specialist
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 Infectious scleritis.
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Disease timeline:
New trial: Routinely Collected Clinical Data and Evaluation of Antimicrobial Target Attainment
Phase NA trial recruiting.
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Common questions about Infectious scleritis
What is Infectious scleritis?
Infectious scleritis is a rare and serious inflammatory condition of the sclera (the tough, white outer coat of the eye) caused by microbial organisms, including bacteria, fungi, viruses, or parasites. Unlike autoimmune or idiopathic scleritis, infectious scleritis results from direct invasion of the scleral tissue by pathogens. It most commonly occurs following ocular surgery (particularly pterygium surgery with adjunctive mitomycin C or beta-irradiation), ocular trauma, or extension of infection from adjacent structures such as the cornea. Rarely, it may arise from hematogenous spread of sys
At what age does Infectious scleritis typically begin?
Typical onset of Infectious scleritis is adult. Age of onset can vary across affected individuals.
Which specialists treat Infectious scleritis?
5 specialists and care centers treating Infectious scleritis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.