Diffused Episclertis |
Episcleritis is simply the Inflammation of the episclera-a thin,
dense vascularised layer of connective tissue which covers the white part of
the eye (sclera). Typically, episcleritis is benign, self-limiting (runs a
limited course of 10 days to weeks and resolves spontaneously) and usually
resolves on its own. Sometimes it may be accompanied by other diseases, such as
lupus, gout, rosacea, psoriasis and rheumatoid arthritis.
It has also been considered as a hypersensitivity reaction to endogenous or streptococcal toxins.
It has also been considered as a hypersensitivity reaction to endogenous or streptococcal toxins.
- Acute onset of mild eye pain.
- Foreign body or gritty sensation.
- Occasional mild watery eyes.
- Increased sensitivity to light (photophobia).
- Eye tenderness.
Nodular Episceritis |
There are actually two types of episcleritis, one in which the episceral redness is diffuse (diffuse episcleritis), and the other in which the episcleral redness is localized (nodular episcleritis). Most people with this eye condition may experience it recurrently and sometimes it comes with no identifiable cause although small fraction of cases is associated with various systemic diseases. Episcleritis is not accompanied by any from purulent discharge and the patient vision is unaffected. Rarely, episcleritis may be caused by scleritis.
Because episcleritis
has a self-limiting characteristics and produces little or no permanent damage
to the eye, many, if not most, patients with this eye condition will not
require any treatment. However, for patients with mild-to-moderate symptoms, cold
compresses over the closed eyelids and instillation of lubricating eye drops
maybe used as a treatment option to decrease the eye discomfort. In more severe cases treatment may involve
the use of topical corticosteroids or oral non-steroidal anti-inflammatory
medications (NSAIDs).
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