Jerry A Shields1, George N Magrath1, Carol Shields1, Richard Mackool2, Ralph C Eagle3, Hans E Grossniklaus4. 1. Ocular Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pa, USA. 2. Mount Sinai New York Eye and Ear Infirmary, New York, N.Y., USA; New York University Medical Center, New York, N.Y., USA. 3. Pathology Department, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pa, USA. 4. Department of Ophthalmic Pathology, Emory University, Atlanta, Ga, USA.
Abstract
PURPOSE: The aim of this study is to report the clinical features, imaging studies, surgical removal, and pathology of congenital iris flocculi in a patient who developed a life-threatening dissecting aortic aneurysm after 55 years of follow-up. METHODS: Documentation with iris photography was performed from age 18 to 55 years, at which time anterior segment optical coherence tomography (OCT) was performed. At the time of subsequent cataract surgery, the iris flocculi were removed in each eye and submitted for light and electron microscopy. RESULTS: The size and shape of the iris flocculi waxed and waned over the years but caused no visual disturbance. Anterior segment OCT demonstrated clear, round cysts with thin lining and no solid component. At the age of 55, congestive heart failure from a dissecting aortic aneurysm was discovered and surgically repaired. Subsequent bilateral cataract surgery and cyst removal were performed, and the iris flocculi were studied with light and electron microscopy. CONCLUSIONS: Congenital iris flocculi cause little, if any, visual impairment in most cases. However, they are occasionally associated with dissecting aortic aneurysm due to a shared mutation in smooth muscle that affects both the iris and the aorta. Patients with iris flocculi should be monitored periodically for aortic abnormalities.
PURPOSE: The aim of this study is to report the clinical features, imaging studies, surgical removal, and pathology of congenital iris flocculi in a patient who developed a life-threatening dissecting aortic aneurysm after 55 years of follow-up. METHODS: Documentation with iris photography was performed from age 18 to 55 years, at which time anterior segment optical coherence tomography (OCT) was performed. At the time of subsequent cataract surgery, the iris flocculi were removed in each eye and submitted for light and electron microscopy. RESULTS: The size and shape of the iris flocculi waxed and waned over the years but caused no visual disturbance. Anterior segment OCT demonstrated clear, round cysts with thin lining and no solid component. At the age of 55, congestive heart failure from a dissecting aortic aneurysm was discovered and surgically repaired. Subsequent bilateral cataract surgery and cyst removal were performed, and the iris flocculi were studied with light and electron microscopy. CONCLUSIONS:Congenital iris flocculi cause little, if any, visual impairment in most cases. However, they are occasionally associated with dissecting aortic aneurysm due to a shared mutation in smooth muscle that affects both the iris and the aorta. Patients with iris flocculi should be monitored periodically for aortic abnormalities.
Authors: Dong-Chuan Guo; Hariyadarshi Pannu; Van Tran-Fadulu; Christina L Papke; Robert K Yu; Nili Avidan; Scott Bourgeois; Anthony L Estrera; Hazim J Safi; Elizabeth Sparks; David Amor; Lesley Ades; Vivienne McConnell; Colin E Willoughby; Dianne Abuelo; Marcia Willing; Richard A Lewis; Dong H Kim; Steve Scherer; Poyee P Tung; Chul Ahn; L Maximilian Buja; C S Raman; Sanjay S Shete; Dianna M Milewicz Journal: Nat Genet Date: 2007-11-11 Impact factor: 38.330