Rheumatology
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Rheumatological diseases which may cause eye disease:
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Rheumatoid arthritis
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Inflammation in sclera – scleritis
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Seronegative arthritides – HLA-B27 positive
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Ankylosing spondylitis, Reiter’s disease
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ïƒ anterior uveitis
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Sjögren’s syndrome
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Dryness of cornea
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Juvenile idiopathic arthritis
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Anterior uveitis in children
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Behcet’s disease
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Devastating panuveitis
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Sarcoidosis
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Intraocular inflammation
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SLE
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Granulomatosis with polyangiitis
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Giant cell arteritis
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Some features that may present:
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Dry eyes
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RA, (can cause secondary Sjögren’s)
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Episcleritis
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Mainly rheumatoid arthritis
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Image to right shows localised area of superficial redness
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Not particularly painful, may have some discomfort
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Segmentally red rather than entire sclera; may just be nasal or temporal aspect
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Managed with lubricants or short course of anti-inflammatory medication
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Uveitis
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Behcet’s, sarcoidosis, JIA
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Retinal vascular occlusion
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SLE
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Orbital disease/ inflammation
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Granulomatosis with polyangiitis
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Anterior ischaemic optic neuropathy (can also present with CRAO)
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GCA
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Ankylosing spondylitis
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Classical patient with ankylosing spondylitis in image to right – disease of lower back
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Typical x-rays on right hand side
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Associated with recurrent bilateral sequential anterior uveitis; tends to affect one eye then second eye etc.
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Detected by ophthalmologist with slit lamp by microscopy
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Image to right shows front of eye
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Irregular pupil = posterior synechiae
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Usually clear aqueous in anterior chamber is replaced by inflammatory exudate which is sticky; adhesions form between iris and anterior lens capsule
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As iris is stuck down, it is unable to fully dilate; patient has probably had dilating eye drops; where eye has tried to dilate, superiorly the links between the iris and anterior lens capsule have broken; iris is trying to pull away. Lump of pigment where iris was previously stuck to lens
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Can cause visual symptoms, degree of eye strain as in discomfort as eye tries to dilate
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Break links with topical cycloplegic such as cyclopentolate (to dilate eye)
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Behcet’s disease
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Idiopathic multisystem disorder
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Occlusive vasculitis – eyes involved in 75%
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Presents in the 3rd and 4th decades
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Diagnosis: oral ulceration with two of:
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Recurrent genital ulceration
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Skin lesions – folliculitis, erythema nodosum
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Positive pathergy test
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Eye involvement
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Acute anterior uveitis
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Vitritis, vasculitis, retinitis
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Treatment, systemic immunosuppression
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Devastating, potentially blinding condition of young adult
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Not common in UK, tends to affect countries in old silk route – China, to Mediterranean
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Some of the features:
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Hypopyon in uveitis
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Retinal vasculitis on dilated examination
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Areas of sheathing of blood vessels (fundus fluorescein angiogram in bottom right – inject with dye, take images with special filter on lens)
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Other systemic tests
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Oral ulcers
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Genital ulcer
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Positive pathergy test – pustule reaction following breaking of skin with needle
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Giant cell arteritis
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Risk of blindness from anterior ischaemic optic neuropathy
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Risk of systemic involvement including cerebrovascular accident – strokes or MIs
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Often preceding history of amaurosis
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Temporal headaches, jaw claudication, weight loss, night sweats, transient visual obscurations
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Associated with polymyalgia rheumatica
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Will affect other eye in 70% if not diagnosed and treatment
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