Outer Retinal Columnar Abnormalities (ORCA): a novel optical coherence tomography sign of CRB1 maculopathy?
Purpose: To report a novel optical coherence tomography (OCT) sign in the context of CRB1 -related maculopathy, termed outer retinal columnar abnormalities (ORCA). Methods: Retrospective, multicenter observational case series of 14 eyes of 8 patients with molecularly confirmed CRB1 -related maculopa...
Published in: | Retina |
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Main Authors: | , , , , , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Ovid Technologies (Wolters Kluwer Health)
2024
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Subjects: | |
Online Access: | http://dx.doi.org/10.1097/iae.0000000000004223 https://journals.lww.com/10.1097/IAE.0000000000004223 |
Summary: | Purpose: To report a novel optical coherence tomography (OCT) sign in the context of CRB1 -related maculopathy, termed outer retinal columnar abnormalities (ORCA). Methods: Retrospective, multicenter observational case series of 14 eyes of 8 patients with molecularly confirmed CRB1 -related maculopathy and ORCA. Multimodal imaging scans and medical records patients with CRB1 -related maculopathy were reviewed. Outcome measures included best-corrected visual acuity (BCVA), central subfield thickness on spectral-domain OCT (SD-OCT), presence of ORCAs and analysis of their change in appearance over time. Results: At baseline, mean age was 18 +/- 10 years (range 9-36). All patients had an isolated macular dystrophy except for 1 case harboring a triallelic pathogenic variant. Variant c.498_506del was found in 9 cases (88%). At presentation, ORCA were visible on macular SD-OCT in all cases as multiform, vertical hyperreflective columnar alterations extending from the ellipsoid to the outer plexiform layer, with a variable degree of hyporeflective cystic spaces in the outer and inner nuclear layers. Over 6 +/- 4.7 follow-up years, the presence of ORCA varied greatly with a decrease in ORCA associated with sequential development of retinal atrophy. Conclusions: A high suspicion for CRB1 -associated retinal dystrophy should arise in the presence of ORCA on SD-OCT, prompting genetic testing. |
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