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Titlebook: Vascular Tumors and Malformations of the Ocular Fundus; J. J. Laey,M. Hanssens Book 1990 Belgian Society of Ophthalmology, Leuven, Belgium

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,Coats’ syndrome and retinitis pigmentosa,ad always complained of night blindness. She presented a total cataract in her left eye. Her right eye had a vision of 1/10 and a tubular visual field. The fundus was typical of retinitis pigmentosa but in the temporal periphery retinal neovascularization, aneurysms and exudates were also noted.
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,Presumed acquired retinal angiomatosis (Adult Coats’ disease),ngiectasis. Leber-Coats’ disease mainly occurs in younger individuals. However, an ophthalmoscopic aspect characterized by retinal vascular anomalies and progressive exudation may also be found in adults [6, 17].
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978-94-010-6753-9Belgian Society of Ophthalmology, Leuven, Belgium and Kluwer Academic Publishers 1990
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Cavernous hemangioma of the retina and of the optic disc,n Hippel’s disease [30]. Up to now, about 80 cases have been published [1–3, 5, 7–21, 23–53]. Cavernous hemangiomas of the retina and of the optic disc are probably congenital non-progressive tumors, which may be part of an oculo-neuro-cutaneous syndrome.
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Choroidal hemangioma,ngioma as a cavernous spindle cell sarcoma. However, it is mainly since the publications by Panas & Remy [52], by Miller [46] and by Nordenson [49] that this tumor has been clinically recognized. Although Reese [56] in 1963 could only trace 128 cases of choroidal hemangiomas in the literature, these
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,Retinal angiomatosis — von Hippel-Lindau’s Disease,hed the description and drawings of the classical red peripheral tumor with the typically dilated artery and veins, but considered the lesion to be an arterio-venous aneurysm [23]. Collins (1894) gave the first pathological description of thin-walled vessels and cystic spaces, but called it a capill
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