e-ISSN: 2717-7149
  • Home
  • About The Journal
  • Editorial Board
  • Instructions for Authors
  • Contact
Current Issue
Ahead Of Print
Archive
Search
Most Popular
Download Articles Read Articles
Retina Arter Tıkanıklıkları ve Tedavisi...
Santral Retinal Ven Tıkanıklığı Güncel Tedavisi...
Central Retinal Artery Occlusion As the Cause of Unilateral Concentric Narrowing of Visual Field and Presence of Cilioretinal Artery...
Bilateral Optic Disc Drusen
Vascular Endothelial Growth Factor and Anti VEGF Agents...
Central Retinal Artery Occlusion As the Cause of Unilateral Concentric Narrowing of Visual Field and Presence of Cilioretinal Artery...
Retina Arter Tıkanıklıkları ve Tedavisi...
Morning Glory Syndrome Associated with Retinochoroidal Coloboma...
Santral Retinal Ven Tıkanıklığı Güncel Tedavisi...
Bilateral Optic Disc Drusen
PureSee Kesintisiz Yüksek Kalitede Görüş
Retina-Vitreous 2012 , Vol 20 , Num 2
Turkish Abstract Abstract Article PDF Similar Articles Mail to Author
Fundus Imagıng of Two Type 2a Juxtafoveal Retinal Telangiectasia Patients
Abdullah ÖZKAYA1, Yaprak Banu ÜNVER2, Nur ACAR3, Ziya KAPRA2
1M.D., Beyoğlu Eye Training and Research Hospital 2nd Eye Clinic, İstanbul/TURKEY
2M.D. Associate Professor, Beyoğlu Eye Training and Research Hospital 2nd Eye Clinic, İstanbul/TURKEY
A 52-year-old woman presented with diminishing vision who had been followed-up with the diagnosis of macular hole by another clinic. Best corrected visual acuity (BCVA) was 20/800 and 20/100, in the right and left eye, respectively. Fundus examination in both eyes revealed macular hole-like image and gray reflection in the fovea. Internal limiting membrane (ILM) drape was detected via optical coherence tomography (OCT) in the fovea in both eyes. Fundus fluorescein angiography (FA) showed telangiectasis in both eyes. Fundus autofluorescence (FOF) imaging revealed hyperautofluorescence in both eyes. A 65-year-old male patient was admitted because of low vision who had been followed-up with a diagnosis of age-related macular degeneration by another clinic. BCVA was 20/400 and 20/800 in the right and left eye, respectively. In both eyes, the fundus examination revealed retina pigment epithelium abnormalities and gray reflection at the fovea. ILM drape, and inner and outer cystic changes were detected in the right eye and inner and outer cystic changes were detected in the left eye via OCT. FFA showed telangiectasis and FOF imaging showed hyperautofluoresence in both eyes. In the light of these findings the patients were assessed as type 2 JFT and taken under observation. JFTs, despite having been described as telangiectasis, are a heterogeneous group of disorders. Type 1 JFT consists of real telangiectatic changes, type 2 JFT represents foveal atrophy, and type 3 remains with foveal ischemia. As in these patients, appropriate examination and differential diagnosis by using imaging techniques can differentiate JFT from other macular diseases and will help us to avoid unnecessary treatment. Keywords : Fundus fluorescein angiography, fundus autofluorescence, juxtafoveal retinal telangiectasia, optical coherence tomography
PureSee Kesintisiz Yüksek Kalitede Görüş
Home
About The Journal
Editorial Board
Instructions for Authors
Contact