Supplementary Material for: Combined Hamartoma of the Retina and Retinal Pigment Epithelium: the contribution of OCT in redefining its development and natural history. A case series.
Version 1Background: Combined hamartoma of the retina and retinal pigment epithelium (CHRRPE) is a rare, benign retinal tumor typically diagnosed in childhood and traditionally believed to involve the full thickness of the retina and the retinal pigment epithelium from early stages. With the advent of optical coherence tomography (OCT), increasing evidence suggests that the primary origin of these lesions may lie within the inner retinal layers, with progressive outward extension over time. However, repo
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Background: Combined hamartoma of the retina and retinal pigment epithelium (CHRRPE) is a rare, benign retinal tumor typically diagnosed in childhood and traditionally believed to involve the full thickness of the retina and the retinal pigment epithelium from early stages. With the advent of optical coherence tomography (OCT), increasing evidence suggests that the primary origin of these lesions may lie within the inner retinal layers, with progressive outward extension over time. However, repo