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DOI: 10.1055/a-2500-5687
Long-term Follow-up of Outer Retinal Microdefects (ORMDs) in Pachychoroid Pigment Epitheliopathy (PPE) and Subsequent Central Serous Chorioretinopathy (CSCR): A Report of Two Cases
Langzeitverlauf von Mikrodefekten der äußeren Netzhaut (ORMD) bei Pachychoroid-Pigmentepitheliopathie (PPE) und nachfolgender zentraler seröser Chorioretinopathie (CSCR): ein Bericht über 2 Fälle
Background
Outer foveal microdefects (OFMDs) are outer retinal abnormalities, typically localized in the foveal or juxtafoveal region [1]. These defects feature focal disruptions in photoreceptor (PR) layers, particularly affecting the ellipsoid zone (EZ) and interdigitation zone (IZ), and may occur alone or with external limiting membrane (ELM) or retinal pigment epithelium (RPE) disruptions. OFMDs, also referred to as macular microholes or foveal spots, and are observed in various hereditary, degenerative, traumatic, and toxic chorioretinal diseases [1], [2].
We report two cases with long-term follow-up of both foveal and extrafoveal microdefects, termed outer retinal microdefects (ORMDs), that differ from typical OFMD, associated with pachychoroid pigment epitheliopathy (PPE) and subsequent central serous chorioretinopathy (CSCR), and demonstrate progressive changes over time.
Publication History
Received: 26 October 2024
Accepted: 09 December 2024
Article published online:
27 February 2025
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References
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