انت هنا الان : شبكة جامعة بابل > موقع الكلية > نظام التعليم الالكتروني > مشاهدة المحاضرة
الكلية كلية الطب
القسم الجراحة
المرحلة 5
أستاذ المادة قاسم كاظم فرهود الربيعي
25/05/2017 07:01:38
Eye and systemic diseases
Thyroid ophthalmopathy: The ocular signs of thyroid diseases arise from 2 sources: 1: sympathetic over activity that causing many of eyelid signs 2: increase volume of orbital contents Signs: Lid lag and lid retraction Orbital congestion Exophthalmos which is either unilateral or bilateral Extra ocular muscles involvement which include the followings: - Enlargement of muscles due to increase muco- polysaccharide content, (the size of the muscles may reach 6 times than the normal) -contracture of the muscles involving the inferior rectus, the medial rectus result in limitation of ocular movement (restrictive myopathy) e- Corneal involvement which include: Exposure keratitis and ocular irritation as a result of rapid dryness of tear film F-Optic nerve involvement: including papillitis and papilloedema Parathyroid gland diseases: Hypercalcemia: Ocular findings: - ca crystals deposition in cornea and conjunctiva Band shape keratopathy( in palpebral fissure) Hypocalcaemia: leading to cataract Disease of the blood 1-sickle cell disease: The ocular lesions arise from intra vascular changes in the conjunctiva and retinal blood vessels Conjunctival findings: There are multiple, short comma shaped distorted capillary segments Retinal findings: Arteriolar occlusions , aneurysms, vascular dilatations and fibro vascular proliferations leading to vitreous hemorrhage. 2- Poly cythaemia: The ocular findings related to blood hyper viscosity resulting in dilatation of conjunctival and retinal blood vessels, and central retinal vein occlusion 3-leukaemia: The ocular features arise from infiltrations and hemorrhage involving the conjunctiva, sclera, retina and choroid Clinical features: Dilated tortuous retinal veins, yellow exudates, cotton wool spots, superficial and deep retinal hemorrhage, vitreous hemorrhage, papilloedema and Proptosis Connective tissue disorders Marfan syndrome: it is autosomal dominant Ocular features: ectopia lentes (the lens dislocated upwards and nasally), myopia, retinal detachment and Keratoconus Sjogren syndrome: 90% are females, the patient presented with xerostomia, chronic arthritis and dry eye (kerato conjunctivitis sicca) C-rheumatoid arthritis: Ocular features: Iritis, scleritis may lead to sclera melting (sclera malacia performance) D-Juvenile rheumatoid arthritis: Ocular findings are: Iritis (bilateral), cataract and band shape keratopathy
المادة المعروضة اعلاه هي مدخل الى المحاضرة المرفوعة بواسطة استاذ(ة) المادة . وقد تبدو لك غير متكاملة . حيث يضع استاذ المادة في بعض الاحيان فقط الجزء الاول من المحاضرة من اجل الاطلاع على ما ستقوم بتحميله لاحقا . في نظام التعليم الالكتروني نوفر هذه الخدمة لكي نبقيك على اطلاع حول محتوى الملف الذي ستقوم بتحميله .
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