Unilateral pigmented paravenous retinochoroidal atrophy with retinitis pigmentosa in the contralateral eye: A case report
Autor: | Masaya Fukushima, Asako Ogawa, Tatsuya Inoue, Mari Kusakabe, Motoshi Yamamoto, Shuichiro Aoki, Kohdai Kitamoto, Ryo Obata |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
medicine.medical_specialty genetic structures Retinitis pigmentosa (RP) 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Atrophy lcsh:Ophthalmology Pigmented paravenous retinochoroidal atrophy (PPRCA) Ophthalmology Case report Retinitis pigmentosa Pigment accumulation medicine Pigmented paravenous retinochoroidal atrophy medicine.diagnostic_test business.industry Retinal Anatomy medicine.disease eye diseases Visual field 030104 developmental biology chemistry lcsh:RE1-994 Visual field test 030221 ophthalmology & optometry sense organs Pigmented Epithelium business |
Zdroj: | American Journal of Ophthalmology Case Reports American Journal of Ophthalmology Case Reports, Vol 8, Iss C, Pp 14-17 (2017) |
ISSN: | 2451-9936 |
DOI: | 10.1016/j.ajoc.2017.08.003 |
Popis: | Purpose We describe a sporadic case of unilateral pigmented paravenous retinochoroidal atrophy (PPRCA) with retinitis pigmentosa (RP) in the contralateral eye. Observations a 24-year-old female aware of the narrowing of visual field was examined at our hospital. Funduscopic examination revealed left eye showing retinochroidal atrophy along the retinal veins with pigment accumulation while right eye showing peripheral diffuse retinal pigmented epithelium atrophy with bone spicule pigmentation. Fundus autofluorescence, electroretinogram, visual field test and optic coherent tomography were also performed and obtained results were compatible with funduscopic observation. Conclusions and importance Simultaneous manifestation of PPRCA and RP observed in this case is rare and supports a shared genetic basis between the two diseases. Further genetic investigations are needed to elucidate the etiology and to properly manage PPRCA. |
Databáze: | OpenAIRE |
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