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Pigmentary glaucoma

Identifieur interne : 003503 ( Istex/Curation ); précédent : 003502; suivant : 003504

Pigmentary glaucoma

Auteurs : Thomas A. Lutz [États-Unis]

Source :

RBID : ISTEX:B200AEFD9C1237E30DB50CC73A1F9DA6E04573D9

Abstract

Pigmentary glaucoma is one of the more common forms of secondary open angle glaucoma. It typically affects younger individuals, being more common among myopes, Caucasian men and persons with a family history of glaucoma. It is characterized by pigment dispersion throughout the anterior segment. The biomicroscopic signs of this condition include iris transillumination defects, Krukenberg spindles, and a dense uniform trabecular meshwork pigment band, oftentimes with a discernable pigmented Schwalbe's line (Sampoalesi line). In addition, pigment deposition may be observed on the anterior iris surface, zonules and the crystalline lens. The development of pigmentary glaucoma moves through a continuum of stages. It is advocated that posterior bowing of the iris (reverse pupillary block) results in iridozonular contact, causing release of iris pigment, i.e. pigmentary dispersion syndrome. Pigment accumulation within the trabecular meshwork leads to endothelial cell damage and loss, resulting in trabecular collapse. The trabecular meshwork support beams collapse and fuse, leading to decreased outflow facility, elevated IOP and glaucoma. Present day management includes antiglaucoma medications, trabeculoplasty, laser iridotomy for those patients with concave iris contour and filtering surgery.

Url:
DOI: 10.1016/S0953-4431(96)00205-6

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ISTEX:B200AEFD9C1237E30DB50CC73A1F9DA6E04573D9

Le document en format XML

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<div type="abstract" xml:lang="en">Pigmentary glaucoma is one of the more common forms of secondary open angle glaucoma. It typically affects younger individuals, being more common among myopes, Caucasian men and persons with a family history of glaucoma. It is characterized by pigment dispersion throughout the anterior segment. The biomicroscopic signs of this condition include iris transillumination defects, Krukenberg spindles, and a dense uniform trabecular meshwork pigment band, oftentimes with a discernable pigmented Schwalbe's line (Sampoalesi line). In addition, pigment deposition may be observed on the anterior iris surface, zonules and the crystalline lens. The development of pigmentary glaucoma moves through a continuum of stages. It is advocated that posterior bowing of the iris (reverse pupillary block) results in iridozonular contact, causing release of iris pigment, i.e. pigmentary dispersion syndrome. Pigment accumulation within the trabecular meshwork leads to endothelial cell damage and loss, resulting in trabecular collapse. The trabecular meshwork support beams collapse and fuse, leading to decreased outflow facility, elevated IOP and glaucoma. Present day management includes antiglaucoma medications, trabeculoplasty, laser iridotomy for those patients with concave iris contour and filtering surgery.</div>
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