| Literature DB >> 23410814 |
Marcela Lonngi1, Aaron S Gold, Timothy G Murray.
Abstract
Retinal astrocytic hamartoma or retinal astrocytoma is the best-known ocular manifestation of tuberous sclerosis complex, a neurocutaneous syndrome characterized by the development of multiple disseminated hamartomas. It can have several clinical presentations, ranging from unilateral transparent, noncalcified lesions to bilateral multinodular, mulberry-like calcified tumors. Symptoms appear if the tumor involves the macula and can cause visual loss on the basis of progressive retinal degeneration. The authors report a case of a patient with tuberous sclerosis, bilateral astrocytic hamartomas, and macular edema with intraretinal hemorrhage in the left eye that has responded well to treatment with bevacizumab and intravitreal triamcinolone acetonide. Copyright 2013, SLACK Incorporated.Entities:
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Year: 2013 PMID: 23410814 DOI: 10.3928/23258160-20121221-19
Source DB: PubMed Journal: Ophthalmic Surg Lasers Imaging Retina ISSN: 2325-8160 Impact factor: 1.300