Retinal astrocytic hamartoma in a patient with Leber's congenital amaurosis
نویسندگان
چکیده
منابع مشابه
Retinal astrocytic hamartoma in a patient with Leber's congenital amaurosis.
To cite: Ambiya V, Kuppermann BD, Narayanan R. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2014208374 DESCRIPTION Retinal astrocytic hamartomas are rare benign tumours that can arise from any location in the retina or from the optic nerve head. Multifocal and bilateral lesions are likely to be associated with tuberous sclerosis and neurofibromatosis 2 but are ...
متن کاملRetinal astrocytic hamartoma.
Routine ophthalmoscopic examination of an asymptomatic, otherwise healthy 63 year old woman revealed a one and a half optic disc diameter sized lesion in the peripheral retina of the right eye (fig 1). The lesion was a greyish white raised nodular mass with patchy calcification overlying the blood vessels on the surface of the retina. The lesion looked more prominent when red-free light was use...
متن کاملMultimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment Epithelium.
Multimodal Imaging of... Klin Monatsbl Augenheilkd hamartoma or the splenic hamartoma. The exact incidence of retinal astrocytic hamartoma (RAH) is not well known, but it is estimated at one case per 100000 births per year [1]. The astrocytic hamartoma is a neuroglial tissue and produces astrocytes within the optic nerve [2], and consequently it often appears within papillary region. Congenital...
متن کاملLebers Amaurosis in Three Siblings: A case report
Retinitis pigmentosa (RP) is the generic name for a group of hereditary disorders characterized by progressive loss of photoreceptors and RPE function. The classical triad of retinitis pigmentosa is arteriolar attenuation, retinal bone spicule pigmentation and waxy disc pallor. Lebers congenital amaurosis (LCA) is the hereditary form of retinitis pigmentosa. It presents with blindness either at...
متن کاملcombined hamartoma of the retina and retinal pigment epithelium in a patient with fundus flavimaculatus
aim: to report a patient with fundus flavimaculatus or macular dystrophy with flecks, who came to medical attention due to deteriorated vision in one eye and combined hamartoma of the retina and retinal pigment epithelium. case presentation: a 26 year old lady was referred with history of progressive decreased vision in both eyes since childhood with recently deteriorated vision in her right ey...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Case Reports
سال: 2015
ISSN: 1757-790X
DOI: 10.1136/bcr-2014-208374