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Punctate Inner Choroidopathy

Journal

SURVEY OF OPHTHALMOLOGY
Volume 56, Issue 1, Pages 36-53

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.survophthal.2010.03.009

Keywords

acute posterior multifocal placoid pigment epitheliopathy; acute zonal occult outer retinopathy; anti-angiogenic factors; birdshot retinochoroidopathy; choroidal neovascular membrane; diffuse subretinal fibrosis syndrome; multifocal choroiditis and panuveitis; multiple evanescent white dot syndrome; photodymanic therapy; presumed ocular histoplasmosis syndrome; punctate inner choroidopathy; serpiginous choroiditis; white-dot syndromes

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Punctate inner choroidopathy (PIC) is a relatively uncommon inflammatory multifocal chorioretinopathy that affects predominantly young myopic women. It is characterized by the presence of multiple, small, well-defined, yellow-white fundus lesions frequently limited to the posterior pole in the absence of flare and inflammatory cells in the anterior chamber or vitreous cavity. Most patients with PIC do not require treatment, as the disease does not often threaten vision; however, when subfoveal choroidal neovascular membrane (CNV) ensues, patients usually lose sight rapidly, requiring immediate care. Treatment modalities that have been used to manage patients with PIC and subfoveal CNV include systemic and local steroids, other immunosuppressant agents, laser photocoagulation, photodynamic therapy, submacular surgery and, most recently, anti-vascular endothelial growth factor therapy. To date, however, there is no clear consensus on the effective therapy. Further research into this area, as well as on the cause and possible predisposing factors for PIC, is warranted. (Surv Ophthalmol 56:36-53, 2011. (C) 2011 Elsevier Inc. All rights reserved.)

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