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Posterior Uveitis Mehmet Can ERATA The Anatomy and Physiology of Uvea-1 What is uvea? The uvea (Lat. Uva, grape), also called the uveal layer, coat, tract or vascular tunic, is the pigmented middle of the three concentric layers that make up of an eye. The uvea consists of three parts (from front to back); Iris (Anterior uvea) Ciliary Body (Intermediate uvea) Choroid (Posterior uvea) The Anatomy and Physiology of Uvea-2 Iris (Anterior uvea): It separates anterior from posterior chamber. It also changes the diameter of the pupilla. Ciliary Body (Intermediate uvea): It produces aqueous humor and determines the focus of the eye via the lens. Choroid (Posterior uvea):The choroid provides oxygen and nourishment to the outer layers of the retina so if it is somehow affected, due to altered oxygenation, vision loss may also occur. Posterior Uveitis (Choroiditis) As you would understand, choroiditis means the inflammation of this middle pigmented and vascular layer of the eye. Posterior uveitis is the rare form of the disorder BUT correct and rapid diagnosis is very important as it is the type of uveitis mostly associated with the loss of vision. The other two forms are more common, and more frequently result in acute symptoms, but only rarely cause vision loss. Sign and Symptoms More subtle eye symptoms are important for the diagnosis as it excludes anterior uveitis and makes us suspect from the diagnosis. (which symptoms are; eye pain, redness, light sensitivity and.). We don’t expect to see eye pain because choroid is not innervated by pain fibers. Floaters, small pecks, flakes or clouds that move through the field of vision and decreased and/or blurred vision. Causes/Differential Diagnosis Behçet’s Disease-1 Behçet's disease or Behçet disease, sometimes called Behçet's syndrome, Morbus Behçet, Behçet-Adamantiades syndrome,or Silk Road disease, is a rare(but very common in Turkey 20421/100.000) immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. Behçet's disease (BD) was named in 1937 after the Turkish dermatologist Hulusi Behçet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis. Behçet’s Disease-2 As a systemic disease, it can also involve visceral organs such as the gastrointestinal tract, pulmonary, musculoskeletal, cardiovascular and neurological systems. This syndrome can be fatal due to ruptured vascular aneurysms or severe neurological complications. Aside from other rheumatological disorders which causes anterior uveitis, Behçet Syndrome ,as a cause of posterior uveitis( as anterior and panuveitis) and major cause of blindness in Turkey, should be very tightly followed up by ophthalmology clinics. Posterior Uveitis-Diagnosis Ophthalmoscopy; one or multiple choroiditis foci which are, in acute phase confluent and white spots. As they heal, they become yellow-brown and acquire more defined borders. It is suggested that only %60 per cent of cases are due to problems that are intrinsic to the eye itself so underlying autoimmune disorders and infections should also be sought/excluded for the diagnosis. Syphilis Toxoplasmosis Behçet’s Disease Complications of Uveitis Glaucoma( via iriditis) Cataracts(via affecting the lens) Cystoid Macular Oedema (swelling of the retina) Detached Retina Posterior Synechiae (iris sticking to the lens) Posterior Uveitis-Treatment The treatment of underlying diagnosis is very important. Posterior uveitis can be treated with either antibiotics or steroids depending on the underlying etiology. References http://behcet.medicine.ankara.edu.tr/?page_id=63 http://rarediseases.org/rare-diseases/posterior-uveitis/ http://www.allaboutvision.com/conditions/uveitis.htm Göz Hastalıkları- El Kitabı/Atlas- Gerhard K. Lang