Literature DB >> 8115732

The dark choroid in systemic argyrosis.

S Y Cohen1, G Quentel, D Egasse, M Cadot, I Ingster-Moati, G J Coscas.   

Abstract

Argyrosis is a cutaneous discoloration caused by silver. Ocular involvement, including conjunctival and corneal discoloration, has been previously reported. To our knowledge, a retinal involvement was never reported and no data is available about fluorescein angiography patterns of patients with argyrosis. Fluorescein angiography was performed in six consecutive patients with iatrogenic systemic argyrosis. A dark choroid was observed in each case. Red light monochromatic pictures disclosed a leopard spot pattern on the fundus, which was more clearly revealed in one patient by infrared light pictures. These findings suggest that the silver deposit in Bruch's membrane may be responsible for the obscuration of choroidal fluorescence during dye transit and for the visualization of choriocapillary units in pictures using long-wavelength light. The dark choroid is not only present in central retinal dystrophies, but may be observed in other conditions, such as systemic argyrosis.

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Year:  1993        PMID: 8115732

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  4 in total

1.  Leopard spot retinal pigmentation in infancy indicating a peroxisomal disorder.

Authors:  C J Lyons; G Castano; A Q McCormick; D Applegarth
Journal:  Br J Ophthalmol       Date:  2004-02       Impact factor: 4.638

2.  A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.

Authors:  K L Anderson; L Baird; R A Lewis; A C Chinault; B Otterud; M Leppert; J R Lupski
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

3.  Ocular argyrosis secondary to long-term ingestion of silver nitrate salts.

Authors:  Kesenia Stafeeva; Michael Erlanger; Raul Velez-Montoya; Jeffrey L Olson
Journal:  Clin Ophthalmol       Date:  2012-12-05

4.  Leopard-like retinopathy and severe early-onset portal hypertension expand the phenotype of KARS1-related syndrome: a case report.

Authors:  Francesca Peluso; Viviana Palazzo; Giuseppe Indolfi; Francesco Mari; Roberta Pasqualetti; Elena Procopio; Claudia Nesti; Renzo Guerrini; Filippo Santorelli; Sabrina Giglio
Journal:  BMC Med Genomics       Date:  2021-01-21       Impact factor: 3.063

  4 in total

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