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      Indocyanine green angiography in pigmented paravenous retinochoroidal atrophy.

      Acta ophthalmologica Scandinavica
      Adult, Atrophy, Child, Choroid, pathology, Choroid Diseases, diagnosis, Coloring Agents, diagnostic use, Disease Progression, Electroretinography, Female, Fluorescein Angiography, Follow-Up Studies, Humans, Indocyanine Green, Male, Middle Aged, Pigment Epithelium of Eye, Retina, Retinal Vein, Retinitis Pigmentosa, Retrospective Studies, Visual Fields

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          Abstract

          To report long-term follow-up of patients with pigmented paravenous retinochoroidal atrophy (PPRCA) and to assess the involvement of the choroid and retinal pigment epithelium (RPE) in PPRCA. Clinical features of PPRCA were studied retrospectively in four patients followed for 6-26 years. Retinal pigment epithelium and choroidal changes were analysed with fluorescein and indocyanine green (ICG) angiography. The two younger patients, aged 16 and 28 years and followed for 6 and 18 years, respectively, showed stationary RPE atrophy and pigmentation. Indocyanine green angiography visualized slight to modest atrophy of the choriocapillaris. The two older patients, aged 69 and 70 years and each followed for 26 years, showed slow progression of disease during follow-up. Indocyanine green angiography revealed choriocapillaris atrophy partly extending into the areas shown as hyperfluorescent in fluorescein angiography. Pigmented paravenous retinochoroidal atrophy is probably a slowly progressive disease, particularly in older patients. The choriocapillaris atrophy in this disease is more properly evaluated by ICG angiography and can be underestimated by fluorescein anigiography.

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