| Literature DB >> 19184312 |
Lihteh Wu1,2, Teodoro Evans3, Mario Saravia4, Ariel Schlaen5, Cristobal Couto5.
Abstract
BACKGROUND: Vogt-Koyanagi-Harada (VKH) syndrome is characterized by bilateral diffuse uveitis associated with auditory, neurological, and cutaneous signs and symptoms. VKH syndrome is a cell-mediated autoimmune disease against melanocytes. Choroidal neovascularization (CNV) occurs in 15% of VKH patients and is associated with poor visual prognosis. CASES: We report on two patients with VKH syndrome and CNV that were treated with intravitreal bevacizumab. OBSERVATIONS: One of the VKH patients also had an extrafoveal CNV membrane and underwent multiple intravitreal injections of bevacizumab in combination with laser photocoagulation, with subsequent improvement in visual acuity. The second had a subfoveal CNV that responded to a single intravitreal injection of bevacizumab.Entities:
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Year: 2009 PMID: 19184312 DOI: 10.1007/s10384-008-0600-4
Source DB: PubMed Journal: Jpn J Ophthalmol ISSN: 0021-5155 Impact factor: 2.447