scholarly journals Subretinal Drusenoid Deposits Revealed by Color SLO and Retro-Mode Imaging

Ophthalmology ◽  
2021 ◽  
Vol 128 (3) ◽  
pp. 409
Author(s):  
Giulia Corradetti ◽  
Federico Corvi ◽  
SriniVas R. Sadda
2018 ◽  
Vol 2 (12) ◽  
pp. 1218-1226 ◽  
Author(s):  
Craig Wilde ◽  
Mary Awad ◽  
Harminder Dua ◽  
Ravi Gandhewar ◽  
Hean-Choon Chen ◽  
...  

Ophthalmology ◽  
2010 ◽  
Vol 117 (9) ◽  
pp. 1775-1781 ◽  
Author(s):  
Sandrine A. Zweifel ◽  
Yutaka Imamura ◽  
Theodore C. Spaide ◽  
Takamitsu Fujiwara ◽  
Richard F. Spaide

2020 ◽  
Author(s):  
Daniel Ahmed ◽  
Martin Stattin ◽  
Anna-Maria Haas ◽  
Alexandra Graf ◽  
Katharina Krepler ◽  
...  

Abstract Background: To assess the relationship between drusen characteristics and type 2 macular neovascularization (MNV) in age-related macular degeneration (AMD)Methods: Retrospective data analysis of eyes previously diagnosed with neovascular AMD in a tertiary eye care center (Medical Retina Unit, Rudolf Foundation Hospital, Vienna, Austria) between June 2008 and December 2017. Drusen subtypes, fibrosis, atrophy and subfoveal choroidal thickness (SFCT) of both eyes in patients with type 2 MNV lesions were categorized based on multimodal imaging.Results: Type 2 MNV was diagnosed in 27 (3.2%) of 835 eyes (749 patients). Drusen characteristics in type 2 MNV were observed as followed: drusen < 63 mm in 2 eyes (7.4%), drusen ≥ 63 mm in 10 eyes (37%), subretinal drusenoid deposits (SDD) in 8 eyes (29.6%), cuticular drusen in 2 eye (7.4%) and no drusen were evident in 10 eyes (37%). Drusen distribution in 23 fellow eyes was detected as followed: drusen < 63 mm in 2 eyes (8.7%), drusen ≥ 63 mm in 9 eyes (39.1%), SDD in 5 eyes (21.7%), cuticular drusen in 1 eye (4.3%) and no drusen were evident in 9 eyes (39.1%). Mean SFCT was 140 ± 49 mm in affected eyes and 152 ± 41 mm in the fellow eyes. Patients with drusen or SDD were significantly younger (mean 70.88 ± 6.85, p=0.04) than patients without deposits (mean 77.40 ± 5.74). Conclusions: Type 2 MNV remains a rare entity in AMD. It was frequently seen in the absence ofdrusen, a hallmark of AMD. These findings contribute to the heterogeneity of phenotypes related to pure type 2 lesions.


2018 ◽  
Vol 2 (8) ◽  
pp. 815
Author(s):  
Yoichi Sakurada ◽  
Ravi Parikh ◽  
Lawrence A. Yannuzzi

2014 ◽  
Vol 158 (3) ◽  
pp. 584-596.e1 ◽  
Author(s):  
Yuhua Zhang ◽  
Xiaolin Wang ◽  
Ernesto Blanco Rivero ◽  
Mark E. Clark ◽  
Clark Douglas Witherspoon ◽  
...  

Retina ◽  
2015 ◽  
Vol 35 (12) ◽  
pp. 2593-2603 ◽  
Author(s):  
Michael J. Heiferman ◽  
Joshua K. Fernandes ◽  
Marion Munk ◽  
Rukhsana G. Mirza ◽  
Lee M. Jampol ◽  
...  

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