Scleritis refers to inflammation of the sclera. It has a wide range of causes.
On this page:
Epidemiology
It can affect any age group but usually those between ages 30 and 50 years. There is a recognized increased female predilection (F:M of ~2:1).
Associations
Scleritis can be associated with systemic infections as well as non-infective systemic conditions which include 1:
rheumatoid arthritis: 18-33%
-
systemic vasculitides: 7-19%
granulomatosis with polyangiitis: most common
Behçet disease: rare 6
sarcoidosis: rare
cryoglobulinaemia: rare
herpes zoster infection: most commonly associated infection
Pathology
Information on the pathogenesis of scleritis is limited due to a lack of published data. However, a predominant role for T cells in the inflammatory process has been postulated 1.
Classification
One widely used classification system is the Watson and Hayreh system which divides scleritis into anterior and posterior forms based upon the anatomic distribution.
-
anterior scleritis (defined by the point of rectus muscle insertion)
diffuse anterior scleritis
nodular anterior scleritis
necrotizing anterior scleritis with inflammation
scleromalacia perforans (necrotizing anterior scleritis without inflammation)
posterior scleritis
Radiographic features
Ultrasound
Ocular ultrasound may play a role in the diagnosis and management of posterior scleritis, demonstrating scleral thickening.
CT/MRI
CT and MRI imaging may also play a role in the diagnosis of scleritis especially during the active phase of the disease. Radiological findings include:7
scleral thickening
scleral enhancement
focal periscleral cellulitis