1996
DOI: 10.1016/s0161-6420(96)30386-2
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Central Serous Chorioretinopathy in Younger and Older Adults

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Cited by 503 publications
(396 citation statements)
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“…[1][2][3][15][16][17][18][19][20][21] In a retrospective study, Mudvari et al 29 found that none of the 340 consecutive CSCR patients developed CNV during an approximate 4-year follow-up period (mean of 49 months). However, Spaide et al 30 reported that older patients with CSCR had a lower VA, and were more likely to have diffuse retinal pigment epitheliopathy and secondary CNV than their younger counterparts. Subsequent reports have suggested that classic CNV (mainly type 2) and polypoidal lesions are possible complications of CSCR and may contribute to visual loss in these eyes.…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3][15][16][17][18][19][20][21] In a retrospective study, Mudvari et al 29 found that none of the 340 consecutive CSCR patients developed CNV during an approximate 4-year follow-up period (mean of 49 months). However, Spaide et al 30 reported that older patients with CSCR had a lower VA, and were more likely to have diffuse retinal pigment epitheliopathy and secondary CNV than their younger counterparts. Subsequent reports have suggested that classic CNV (mainly type 2) and polypoidal lesions are possible complications of CSCR and may contribute to visual loss in these eyes.…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, two reports that showed significant visual improvement with PDT in chronic CSC also used FFA rather than ICG, 14,20 considered essential by others. 2,5,6 TTT has been successfully used to treat subfoveal CNV of various aetiologies. [21][22][23] Owing to its thermal nature, TTT may act like conventional photocoagulation in CSC, causing RPE debridement, migration, transformation, and re-proliferation.…”
Section: Discussionmentioning
confidence: 99%
“…A second uncommon type, with widespread alterations of RPE pigmentation in the posterior pole, is termed 'chronic' or 'diffuse retinal pigment epitheliopathy' (DRPE). 2 This subtype is associated with older age, chronic (46 months) detachment of the posterior pole, poorly defined RPE leakage or 'ooze,' multiple pigment epithelial detachments (PED), and poor visual prognosis owing to cystoid macular oedema, foveolar atrophy, subretinal fibrosis, and less commonly, choroidal neovascularization (CNV). [2][3][4][5][6][7][8] In spite of the innumerable studies on CSC, there is continued controversy in the literature on the need, timing, and choice of treatment.…”
Section: Introductionmentioning
confidence: 99%
“…1 Although the pathogenesis of this condition has been extensively investigated, it remains a matter of controversy. In several hypotheses, choroidal hyperpermeability and dysfunction of RPE have been regarded as strong candidates for the origin of this disorder.…”
Section: Introductionmentioning
confidence: 99%