Polypoidal Choroidal Vasculopathy
- PMID: 33620857
- Bookshelf ID: NBK567780
Polypoidal Choroidal Vasculopathy
Excerpt
Polypoidal choroidal vasculopathy (PCV) is an exudative maculopathy characterized by multiple recurrent serosanguineous retinal pigment epithelial detachments (PED). It is similar to neovascular age-related macular degeneration in morphological characteristics. It was first described by Yannuzzi et al at an annual meeting of the American Academy of Ophthalmology in 1982 and termed idiopathic polypoidal choroidal vasculopathy (IPCV) in 1984, Kleiner et al described a similar presentation in middle-aged black women and named it posterior uveal bleeding syndrome. Later, Yannuzzi et al described PCV in detail and established its existence across genders, various age groups, and races.
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References
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- Kleiner RC, Brucker AJ, Johnston RL. The posterior uveal bleeding syndrome. Retina. 1990;10(1):9-17. - PubMed
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- Yannuzzi LA, Sorenson J, Spaide RF, Lipson B. Idiopathic polypoidal choroidal vasculopathy (IPCV). Retina. 1990;10(1):1-8. - PubMed
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- Lafaut BA, Aisenbrey S, Van den Broecke C, Bartz-Schmidt KU, Heimann K. Polypoidal choroidal vasculopathy pattern in age-related macular degeneration: a clinicopathologic correlation. Retina. 2000;20(6):650-4. - PubMed
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- Sakurada Y, Yoneyama S, Imasawa M, Iijima H. Systemic risk factors associated with polypoidal choroidal vasculopathy and neovascular age-related macular degeneration. Retina. 2013 Apr;33(4):841-5. - PubMed
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- Lip PL, Hope-Ross MW, Gibson JM. Idiopathic polypoidal choroidal vasculopathy: a disease with diverse clinical spectrum and systemic associations. Eye (Lond) 2000 Oct;14 Pt 5:695-700. - PubMed
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