Definition
Polypoidal choroidal vasculopathy (PCV) is a macular disorder characterized by recurrent hemorrhage within the retina and retinal pigment epithelium (RPE). It is characterized by the presence of choroidal vascular channels (also known as the branching vascular network, BVN) ending in polyp-like dilations in the peripapillary and macular area.
Etiology
The etiology is still unknown. There are similarities between the genetic predisposition to PCV and to wet AMD. For example, a functional SNP at the promoter of serine protease HTRA1 was associated with a tenfold increased risk of developing PCV and choroidal neovascularization in Asians. Common causative genes include complement factor H on chromosome 1q23–32, albeit with different SNPs: Y402H (for neovascular AMD); rs3753394, rs800292...
References
Hirami Y et al (2007) Hemorrhagic complications after photodynamic therapy for polypoidal choroidal vasculopathy. Retina 27(3):335–341
Koh A et al (2012) EVEREST study: efficacy and safety of verteporfin photodynamic therapy in combination with ranibizumab or alone versus ranibizumab monotherapy in patients with symptomatic macular polypoidal choroidal vasculopathy. Retina 32(8):1453–1464
Koh AH et al (2013) Polypoidal choroidal vasculopathy: evidence-based guidelines for clinical diagnosis and treatment. Retina 33(4):686–716
Yuzawa M, Mori R, Haruyama M (2003) A study of laser photocoagulation for polypoidal choroidal vasculopathy. Jpn J Ophthalmol 47(4):379–384
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Koh, A. (2014). Polypoidal Choroidal Vasculopathy. In: Schmidt-Erfurth, U., Kohnen, T. (eds) Encyclopedia of Ophthalmology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-35951-4_982-1
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DOI: https://doi.org/10.1007/978-3-642-35951-4_982-1
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Publisher Name: Springer, Berlin, Heidelberg
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