2020
DOI: 10.1007/s10792-020-01620-0
|View full text |Cite
|
Sign up to set email alerts
|

Idiopathic polypoidal choroidal vasculopathy: a review of literature with clinical update on current management practices

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
22
0
1

Year Published

2021
2021
2022
2022

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 8 publications
(23 citation statements)
references
References 82 publications
0
22
0
1
Order By: Relevance
“…Increased inflammation seems to be one of the etiologic key factors in AMD, PCV, and CVD, and different inflammation markers have been shown to be strongly associated with both late AMD and CVD 5,7,22,86 . Moreover, many of the aforementioned risk factors are associated with inflammation and vascular alterations.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Increased inflammation seems to be one of the etiologic key factors in AMD, PCV, and CVD, and different inflammation markers have been shown to be strongly associated with both late AMD and CVD 5,7,22,86 . Moreover, many of the aforementioned risk factors are associated with inflammation and vascular alterations.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies reported an estimated prevalence of over 25% in subjects above the age of 60 years and a 15% increase in AMD incidence in individuals aged 75 years and older 1–3 . Polypoidal choroidal vasculopathy (PCV), a disease highly prevalent in Asian populations, has been considered a variant of neovascular AMD and reported to share similar risk factors 4,5 . AMD is a complex multifactorial disease with genetic and environmental risk factors 2,4–7 .…”
mentioning
confidence: 99%
“…The genetics of PCV are not as well investigated as those of AMD. PCV and AMD share some single nucleotide polymorphisms in complement and inflammatory genes, but other genetic markers unique to PCV could not consistently be identified [1,2] More recently, PCV was classified as part of the pachychoroid disease spectrum, which includes pachychoroid pigment epitheliopathy and central serous chorioretinopathy [3]. This classification is, however, not consistent with PCV being a subtype of AMD.…”
Section: Introductionmentioning
confidence: 99%
“…They may present as singular nodules or multiple grape-like clusters of hyperfluorescence together with atypical choroidal vessels forming branched vascular networks. The EVEREST study and the Japanese Study Group have defined diagnostic criteria based on ICG angiography and funduscopic appearance [1,2]. In contrast to ICG imaging, spectral domain optical coherence tomography (SD-OCT) is noninvasive and more readily available.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation