What is the Difference Between Scleritis and Episcleritis?
🆚 Go to Comparative Table 🆚Scleritis and episcleritis are two different inflammatory conditions that affect the eye. They present with some similar features but have distinct differences:
Episcleritis:
- Inflammation of the superficial, episcleral layer of the eye.
- Relatively common, benign, and self-limiting.
- No identifiable cause in most cases, but some are associated with systemic inflammatory conditions.
- Often recurrent, with attacks typically recurring every few months.
- Nine times more common in women than men.
- Most common in adults in their 40s and 50s.
- Usually resolves over 7-10 days without treatment.
Scleritis:
- Inflammation involving the sclera.
- Severe ocular inflammation, often with ocular complications, and nearly always requires systemic treatment.
- Occurs more commonly in older women and is usually associated with an underlying systemic disease.
- Tends to come on more slowly and affects the deep white layer (sclera) of the eye.
- Can spread to affect adjacent layers around the sclera, including the episclera and the cornea.
- Requires ophthalmology consultation and steroids +/- topical antibiotics for management.
In summary, episcleritis is an inflammation of the superficial episcleral layer and is relatively common, benign, and self-limiting, while scleritis is an inflammation involving the sclera and is a severe and potentially blinding ocular condition that requires systemic treatment. Both conditions can initially look similar but have different clinical presentations and treatments.
Comparative Table: Scleritis vs Episcleritis
Here is a table comparing the differences between scleritis and episcleritis:
Feature | Scleritis | Episcleritis |
---|---|---|
Definition | Inflammation involving the sclera, a severe ocular inflammation | Inflammation of the superficial episcleral layer of the eye, relatively common and benign |
Severity | Often requires systemic treatment, can lead to ocular complications | Self-limiting, typically does not progress to scleritis |
Pain | Significant pain, pain with eye movement, vision loss | Less painful, no vision loss |
Vessel Blanching | Vessels do not blanch with phenylephrine, deeper scleral vessels involved | Vessels blanch with phenylephrine, superficial episcleral vessels involved |
Causes | Often associated with other inflammatory diseases, such as rheumatoid arthritis | Most cases have no identifiable cause, some associated with systemic inflammatory conditions |
Epidemiology | Estimated incidence of 41.0 per 100,000 per year; prevalence of 52 | Incidence estimated at 41.0 per 100,000 per year; prevalence of 52 |
Treatment | Ophthalmology consultation, steroids, and possibly topical antibiotics | Ophthalmology consultation when further investigation is required; usually self-limited and does not require acute treatment |
Types | Nodular, diffuse, necrotizing with inflammation, and necrotizing without inflammation | Simple (diffuse or nodular) |
Both scleritis and episcleritis are clinical diagnoses, and a thorough examination is essential to differentiate between the two conditions.
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