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Ferenczy, S

https://orcid.org/0000-0003-0076-496X

Mayo Clinic

Thomas Jefferson University

Citations 2

White Paper on Ophthalmic Imaging for Choroidal Nevus Identification and Transformation into Melanoma
Lally, Sara E. , Pellegrini, Marco , Kaliki, Swathi , Gündüz, Kaan , Fung, Adrian T. , Duker, Jay S. , Selig, Sara , Yaghy, Antonio , Ferenczy, S , Eydelman, Malvina, Blumenkranz, Mark S. , Shields, Carol L. , Dalvin, Lauren A. , Sagoo, Mandeep S. , Furuta, Minoru , Mruthyunjaya, Prithvi

Translational Vision Science & Technology | February 20, 2021 | Volume: 10 | Issue: 2 | Pages: 24

10.1167/tvst.10.2.24 Get It

SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY FEATURES OF VITREORETINAL LYMPHOMA IN 55 EYES
Yang, Xiaolu , Lim, Li‐Anne , Ancona‐Lezama, David , Shields, Jerry A., Dalvin, Lauren A. , Mazloumi, Mehdi , Ferenczy, S , Mashayekhi, Arman , Shields, Carol L.

Retina | April 29, 2020 | Volume: 41 | Issue: 2 | Pages: 249-258

10.1097/iae.0000000000002819 Get It

Purpose: To evaluate spectral domain optical coherence tomography (SD-OCT) features of vitreoretinal lymphoma (VRL). Methods: Review of records and SD-OCT images of vitreoretinal lymphoma evaluated at Ocular Oncology Service, Wills Eye Hospital between July 1, 2000, and April 1, 2019. Results: There were 55 eyes of 32 patients included. At presentation, SD-OCT features included vitreous opacities (n = 36, 65%), preretinal deposits (n = 7, 13%), intraretinal deposits (n = 8, 15%), subretinal deposits (n = 20, 36%), retinal pigment epithelium abnormalities (n = 35, 64%), and subretinal pigment epithelium deposits (n = 35, 64%). Of 36 eyes with observed tumor progression, comparison (initial visit vs. time of progression) revealed more intraretinal deposits (17% vs. 50%, P = 0.005) at progression. Of 15 eyes with tumor recurrence, comparison (initial visit vs. time of recurrence) revealed more intraretinal deposits (7% vs. 47%, P = 0.04) at recurrence. At last visit, 39 eyes demonstrated tumor regression. By comparison (initial presentation vs. regression), there were less frequent vitreous opacities (67% vs. 0%, P < 0.001), intraretinal deposits (15% vs. 0%, P = 0.03), subretinal deposits (36% vs. 0%, P < 0.001), and subretinal pigment epithelium deposits (69% vs. 21%, P < 0.001) at regression. Conclusion: Using SD-OCT in patients with vitreoretinal lymphoma, local tumor regression correlated with a reduction in vitreous opacities, intraretinal deposits, subretinal deposits, and subretinal pigment epithelium deposits. SD-OCT is useful in judging vitreoretinal lymphoma response to therapy.