Sclera
Scleritis
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Scleritis
, Nodular Scleritis, Necrotizing Scleritis
See Also
Sclera
Episcleritis
Red Eye
Epidemiology
Rare
Pathophysiology
Severe
Sclera
l inflammation
Variations
Nodular Scleritis
Necrotizing Scleritis (most destructive)
Anterior Scleritis (deep to
Conjunctiva
)
Posterior Scleritis (overlying
Retina
)
Causes
Idiopathic in 50% of cases
Connective Tissue Disease
Rheumatoid Arthritis
(most common cause)
Accounts for up to one third of Scleritis cases
Scleritis occurs in 4-10% of RA cases
Granulomatosis with Polyangiitis
(previously known as
Wegener's Granulomatosis
)
Polyarteritis Nodosa
Systemic Lupus Erythematosus
Relapsing Polychondritis
Reiter's Syndrome
Psoriatic Arthritis
Ankylosing Spondylitis
Inflammatory Bowel Disease
Crohn's Disease
Ulcerative Colitis
Infectious (uncommon)
Herpes Zoster
Herpes Simplex Virus
Pseudomonas
Aspergillus
Tuberculosis
Symptoms
Red Eye
involving one or both eyes
Blurred Vision
Photophobia
Subacute course with gradual onset
Significant
Eye Pain
(especially Necrotizing Scleritis)
Deep boring toothace-type
Eye Pain
Pain radiates to eyebrows, cheeks and temples
Pain worse with eye movments
Intense night pain with pain on awakening
Assocated symptoms
Fever
Headache
Vomiting
Signs
Decreased Visual Acuity
Pain on palpation
Diffuse
Eye Redness
Sclera
l edema
Corneal Ulcer
ation
Scleromalacia (severe cases)
Sclera
thins and takes on a bluish hue
Signs
Slit Lamp
Exam
Critical to do this exam prior to
Fluorescein
application
Fluorescein
can settle in the stroma and obscure the Scleritis findings and extent
Localized, raised hyperemia of
Sclera
Elevated
Sclera
l vessels
Scleritis does not blanch with topical
Phenylephrine
Phenylephrine
blurs
Vision
for 3 hours
Phenylephrine
contraindicated in
Glaucoma
Avascular areas over
Sclera
Associated Conditions
Associated with
Rheumatologic Condition
s,
Inflammatory Bowel Disease
in >50% of cases
Anterior Scleritis
Iritis
Glaucoma
Posterior Scleritis
Retinal Detachment
Proptosis
Differential Diagnosis
See
Red Eye
Episcleritis
Conjunctivitis
Management
NSAID
s
Indomethacin
25 mg orally twice daily
Ibuprofen
600 mg orally three times daily
Naproxen
250 to 500 mg orally twice daily
Ophthalmology referral
Advanced cases may require
Immunosuppressant
s and
Corticosteroid
s
Course
Duration of months to years
Complications
Sclera
l thinning or perforation
Staphyloma
Scleromalacia perforans (in
Rheumatoid Arthritis
)
References
Goldstein in Yanoff (1999) Ophthalmology, p. 13.1
Ruddy (2001) Kelley's Rheumatology, Saunders, p. 396
Nakla (1998) Gastroenterol Clin North Am 27:697-711 [PubMed]
Pflipsen (2016) Am Fam Physician 93(12): 991-8 [PubMed]
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