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Spontaneous Collapse of a Primary Iris Cyst Associated With an Iris Nevus

Spontaneous Collapse of a Primary Iris Cyst Associated With an Iris Nevus Abstract Primary iris cysts are unusual ocular abnormalities that may be congenital. We describe a primary iris cyst associated with an iris nevus that spontaneously collapsed within a 1-year followup period. Report of a Case. —A 13-year-old white boy was seen on February 21, 1989, for evaluation of a pigmented iris lesion. The patient had no previous history of ocular surgery or trauma and had not been receiving topical medications. Visual acuity was 20/20 OU. Intraocular pressures and dilated fundus examination results were normal. Slit-lamp examination of the right eye was unremarkable. Slit-lamp examination of the left eye revealed a flat, pigmented lesion occupying a portion of the nasal iris. A focal area of increased pigmentation was present in the adjacent anterior chamber angle by gonioscopy. A round, pigmented iris cyst extending from the References 1. Shields JA, Kline MW, Augsburger JJ. Primary iris cysts: a review of the literature and report of 62 cases . Br J Ophthalmol . 1984;68:152-166.Crossref 2. Duke-Elder S. Diseases of the Uvea: System of Ophthalmology . St Louis, Mo: CV Mosby Co; 1974:762. 3. Sihota R, Tiwari HK, Azad RV, Khosla PK. Photocoagulation of large iris cysts . Ann Ophthalmol . 1988;20:470-472. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Ophthalmology American Medical Association

Spontaneous Collapse of a Primary Iris Cyst Associated With an Iris Nevus

Archives of Ophthalmology , Volume 109 (1) – Jan 1, 1991

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References (3)

Publisher
American Medical Association
Copyright
Copyright © 1991 American Medical Association. All Rights Reserved.
ISSN
0003-9950
eISSN
1538-3687
DOI
10.1001/archopht.1991.01080010023015
Publisher site
See Article on Publisher Site

Abstract

Abstract Primary iris cysts are unusual ocular abnormalities that may be congenital. We describe a primary iris cyst associated with an iris nevus that spontaneously collapsed within a 1-year followup period. Report of a Case. —A 13-year-old white boy was seen on February 21, 1989, for evaluation of a pigmented iris lesion. The patient had no previous history of ocular surgery or trauma and had not been receiving topical medications. Visual acuity was 20/20 OU. Intraocular pressures and dilated fundus examination results were normal. Slit-lamp examination of the right eye was unremarkable. Slit-lamp examination of the left eye revealed a flat, pigmented lesion occupying a portion of the nasal iris. A focal area of increased pigmentation was present in the adjacent anterior chamber angle by gonioscopy. A round, pigmented iris cyst extending from the References 1. Shields JA, Kline MW, Augsburger JJ. Primary iris cysts: a review of the literature and report of 62 cases . Br J Ophthalmol . 1984;68:152-166.Crossref 2. Duke-Elder S. Diseases of the Uvea: System of Ophthalmology . St Louis, Mo: CV Mosby Co; 1974:762. 3. Sihota R, Tiwari HK, Azad RV, Khosla PK. Photocoagulation of large iris cysts . Ann Ophthalmol . 1988;20:470-472.

Journal

Archives of OphthalmologyAmerican Medical Association

Published: Jan 1, 1991

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