Unilaterale pigmentierte paravenöse retinochorioidale atrophie

P. Charbel Issa; Hendrik P.N. Scholl; H. M. Helb; M. Fleckenstein; C. Inhetvin-Hutter; F. G. Holz

doi:10.1055/s-2007-963600

Unilaterale pigmentierte paravenöse retinochorioidale atrophie

Translated title of the contribution: Unilateral pigmented paravenous retinochoroidal atrophy

P. Charbel Issa, Hendrik P.N. Scholl, H. M. Helb, M. Fleckenstein, C. Inhetvin-Hutter, F. G. Holz

Research output: Contribution to journal › Short survey › peer-review

12 Scopus citations

Abstract

We report the case of an asymptomatic unilateral pigmented paravenous retinochoroidal atrophy (PPRCA) in a 43-year-old patient. The right eye showed chorioretinal atrophy with bone-spicule-like pigmentations along the retinal veins. Visual acuity was 20/20 and perimetry revealed scotomas correlating to the chorioretinal atrophy. Electrophysiological examination showed decreased signals in ERG and EOG. Fundus autofluorescence and angiography findings are presented. Pathogenetically, a classification as hereditary retinal dystrophy (as in retinitis pigmentosa) as well as a post-inflammatory residuum are discussed.

Translated title of the contribution	Unilateral pigmented paravenous retinochoroidal atrophy
Original language	German
Pages (from-to)	791-793
Number of pages	3
Journal	Klinische Monatsblatter fur Augenheilkunde
Volume	224
Issue number	10
DOIs	https://doi.org/10.1055/s-2007-963600
State	Published - Oct 2007
Externally published	Yes

Keywords

Angiography
Autofluorescence
Electrophysiology
Pigmented paravenous retinochoroidal atrophy
Retina
Unilateral

ASJC Scopus subject areas

Ophthalmology

Access to Document

10.1055/s-2007-963600

Cite this

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title = "Unilaterale pigmentierte paraven{\"o}se retinochorioidale atrophie",

abstract = "We report the case of an asymptomatic unilateral pigmented paravenous retinochoroidal atrophy (PPRCA) in a 43-year-old patient. The right eye showed chorioretinal atrophy with bone-spicule-like pigmentations along the retinal veins. Visual acuity was 20/20 and perimetry revealed scotomas correlating to the chorioretinal atrophy. Electrophysiological examination showed decreased signals in ERG and EOG. Fundus autofluorescence and angiography findings are presented. Pathogenetically, a classification as hereditary retinal dystrophy (as in retinitis pigmentosa) as well as a post-inflammatory residuum are discussed.",

keywords = "Angiography, Autofluorescence, Electrophysiology, Pigmented paravenous retinochoroidal atrophy, Retina, Unilateral",

author = "{Charbel Issa}, P. and Scholl, {Hendrik P.N.} and Helb, {H. M.} and M. Fleckenstein and C. Inhetvin-Hutter and Holz, {F. G.}",

year = "2007",

month = oct,

doi = "10.1055/s-2007-963600",

language = "German",

volume = "224",

pages = "791--793",

journal = "Klinische Monatsblatter fur Augenheilkunde",

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T1 - Unilaterale pigmentierte paravenöse retinochorioidale atrophie

AU - Charbel Issa, P.

AU - Scholl, Hendrik P.N.

AU - Helb, H. M.

AU - Fleckenstein, M.

AU - Inhetvin-Hutter, C.

AU - Holz, F. G.

PY - 2007/10

Y1 - 2007/10

N2 - We report the case of an asymptomatic unilateral pigmented paravenous retinochoroidal atrophy (PPRCA) in a 43-year-old patient. The right eye showed chorioretinal atrophy with bone-spicule-like pigmentations along the retinal veins. Visual acuity was 20/20 and perimetry revealed scotomas correlating to the chorioretinal atrophy. Electrophysiological examination showed decreased signals in ERG and EOG. Fundus autofluorescence and angiography findings are presented. Pathogenetically, a classification as hereditary retinal dystrophy (as in retinitis pigmentosa) as well as a post-inflammatory residuum are discussed.

AB - We report the case of an asymptomatic unilateral pigmented paravenous retinochoroidal atrophy (PPRCA) in a 43-year-old patient. The right eye showed chorioretinal atrophy with bone-spicule-like pigmentations along the retinal veins. Visual acuity was 20/20 and perimetry revealed scotomas correlating to the chorioretinal atrophy. Electrophysiological examination showed decreased signals in ERG and EOG. Fundus autofluorescence and angiography findings are presented. Pathogenetically, a classification as hereditary retinal dystrophy (as in retinitis pigmentosa) as well as a post-inflammatory residuum are discussed.

KW - Angiography

KW - Autofluorescence

KW - Electrophysiology

KW - Pigmented paravenous retinochoroidal atrophy

KW - Retina

KW - Unilateral

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DO - 10.1055/s-2007-963600

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Unilaterale pigmentierte paravenöse retinochorioidale atrophie

Abstract

Keywords

ASJC Scopus subject areas

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