Journal of the Korean Ophthalmological Society 1995;36(2):355-360.
Published online February 1, 1995.
A Case of Tuberous Sclerosis.
Yoon Jung Ku, Eun Ah Kim, Young Bock Han
Department of Ophthalmology, College of Medicine, I-Hwa Weman University, Seoul, Korea.
Tuberous sclerosis 1 예
구윤정(Yoon Jung Ku),김은아(Eun Ah Kim),한영복(Young Bock Han)
Abstract
Tuberous sclerosis is a heredofamilial disease associated with the diagnostic triad of epilepsy, mental retardation, and skin lesions, adenoma sebaceum. Retinal hamartomas are the most common ocular abnormalities in patients with tuberous sclerosis and are classified as three types: 1) large whitish calcified nodular masses, 2) flat transluscent noncalcified smooth tumors, and 3) intermediate type. We introduce a case on 22 year-old male of tuberous sclerosis who was manifested by epilepsy, adenoma sebaceum without mental retardation. And he was characterized by multiple flat transluscent noncalcified type of retinal astrocytic hamartoma accompanied by Shagreen patch, sclerotic calcification in skull and angiomyolipoma on both kidneys.
Key Words: Tuberous Sclerosis;Retinal hamartoma


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