SavedAdd your journal

Journals / Güncel Retina Dergisi / 2020 / Cilt: 4 - Sayı: 2

Epidemiology, Prevalence and Incidence in Pachychoroid Disease Spectrum

Pakikoroid Spektrum Hastalıklarında Epidemiyoloji, Prevalans ve İnsidans

Emrah KAN
Pages
57–61
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Th aim of this review is to exhibit the epidemiology, incidence and prevalence of the pachychoroid diseases respectively

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Pachychoroid is a relatively novel concept describing a phenotype characterized by increased choroidal thickening, pathologically dilated veins in the Haller’s layer (pachy-veins), thinning in Sattler’s and choriocapilleris layers.
📊
Key Findings & Data:Th spectrum comprises the following disease groups: Pachychoroid Pigment Epitheliopathy (PPE), Central Serous Chorioretinopathy (CSCR), Pachychoroid Neovasculopathy (PNV), Polipoidal Choroidal Vasculopathy (PCV), Focal choroidal excavation (FCE), Peripapillary pachychoroid syndrome (PPS).
💡
Conclusion & Impact:Th aim of this review is to exhibit the epidemiology, incidence and prevalence of the pachychoroid diseases respectively
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Pachychoroid is a relatively novel concept describing a phenotype characterized by increased choroidal thickening, pathologically dilated veins in the Haller’s layer (pachy-veins), thinning in Sattler’s and choriocapilleris layers. Th spectrum comprises the following disease groups: Pachychoroid Pigment Epitheliopathy (PPE), Central Serous Chorioretinopathy (CSCR), Pachychoroid Neovasculopathy (PNV), Polipoidal Choroidal Vasculopathy (PCV), Focal choroidal excavation (FCE), Peripapillary pachychoroid syndrome (PPS). Thse conditions all exhibit the characteristic choroidal alterations and are believed to represent diffrent manifestations of a common pathogenic process. Th aim of this review is to exhibit the epidemiology, incidence and prevalence of the pachychoroid diseases respectively

Özet

Pakikoroid spektrum hastalıkları, Haller tabakasında patolojik olarak damarların genişlemesi (pakivenler), Sattler ve koriokapillaris tabakalarında inceltme ve artmış koroid kalınlığı ile karakterize bir fenotipi tanımlayan nispeten yeni bir konsepttir. Spektrum, aşağıdaki hastalık gruplarını içerir: Santral seroz koriyoretinopati (SSR), Pakikoroid pigment epitelyopati (PPE), Pakikoroid neovaskülopati (PNV), Polipoidal koroidal vaskülopati (PKV), Fokal koroidal ekskavasyon (FKE), Peripapiller pakikoroid sendrom (PPS). Bu hastalıkların koroid yapısında bozukluk ile başlayan ortak bir patojenik sürecin farklı tezahürleri olduğuna inanılmaktadır. Bu derleme, pakikoroid hastalık spektrumunda epidemiyoloji, prevalans ve insidans hakkında, güncel literatür bağlamında mevcut anlayışı vurgulamaktadır.

🔖

Cite This Article

KAN, E. (2020). Epidemiology, Prevalence and Incidence in Pachychoroid Disease Spectrum. Güncel Retina Dergisi, Cilt: 4 - Sayı: 2, 57–61. https://ajindex.com/articles/158912

References (9)

  1. Warrow DJ, Hoang QV, Freund KB. Pachychoroid pigment epitheliopathy. Retina. 2013;33(8):1659–1672
  2. Hirata M, Tsujikawa A, Matsumoto A, Hangai M, Ooto S, Yamashiro K, et al. Macular choroidal thickness and volume in normal subjects measured by swept-source optical coherence tomography. Invest Ophthalmol Vis Sci 2011;52(8): 4971–4978 3. Hosoda YI, Uji A, Hangai M. Relationship between retinal lesions and inward choroidal bulging in Vogt–Koyanagi–Harada disease. Am J Ophthalmol 2014;157(5):1056–1063 4. Dansingani KK, Balaratnasingam C, Naysan J, Freund KB. En face imaging of pachychoroid spectrum disorders with sweptsource optical coherence tomography. Retina. 2016;36(3): 499–516
  3. Ersoz MG, Karacorlu M, Arf S, Hocaoglu M, Sayman Muslubas I. Pachychoroid pigment epitheliopathy in fellow eyes of patients with unilateral central serous chorioretinopathy. Br J Ophthalmol. 2018 Apr;102(4):473-478
  4. Gallego-Pinazo R, Dolz-Marco R, Gómez-Ulla F, Mrejen S, Freund KB. Pachychoroid diseases of the macula. Med Hypothesis Discov Innov Ophthalmol 2014;3(4):111–115 7. Bennet G. Central serous retinopathy. Br J Ophthalmol. 1955;39(10): 605- 618 8. Von Graefe A. Ueber centrale recidivierende Retinitis. Graefes Arch Clin Exp Ophthalmol. 1866;12(1):211-215 9. Gass JDM. Pathogenesis of disciform detachment of the neuroepithelium. II Idiopathic Central Serous Chorioretinopathy. Am J Opthalmol. 1967;63(3):587-615
  5. Wang M, Munch IC. Central serous chorioretinopathy. Acta Opthalmol. 2008;86(2):126-145 11. Kitzmann AS, Pulido JS, Diehl NN, Hodge DO, Burke JP. Th incidence of central serous chorioretinopathy in Olmsted County, Minnesota, 1980- 2002. Ophthalmology. 2008;115(1):169-73
  6. Tsai DC, Chen SJ, Huang CC, Chou P, Chung CM, Huang PH, et al. Epidemiology of idiopathic central serous chorioretinopathy in Taiwan, 2001-2006: a population-based study. PLoS One. 2013; 24;8(6): e66858
  7. Gelber GS, Schatz H. Loss of vision due to central serous chorioretinopathy following psychological stress. Am J Pschiatry. 1987; 144(1):46-50
  8. Spitznas M, Huke J. Number, shape and topography of leakage points in acute type central serous retinopathy. Graefes Arch Clin Exp Opthalmol. 1987;225(6):437-440 15. Castro-Correia J, Coutinho MF, Rosas V. Long-term followup central serous chorioretinopathy in 150 patients. Doc Opthalmologica. 1992;81(4):379-386
  9. Wang M, Sander B. Clinical characteristics of subretinal deposits in central serous chorioretinopathy. Acta Opthalmol Sc