Journal of the Korean Ophthalmological Society 2006;47(10):1696-1702.
Published online October 31, 2006.
A Case of Iridocorneal Endothelial Syndrome with Pigmentary Glaucoma.
Ji Yeon Kim, Ja Heon Kang
1Department of Ophthalmology, Chonbuk National University College of Medicine, Cheonbuk, Korea.
2Department of Ophthalmology, Kyunghee University East-West Neo Medical Center, Seoul, Korea. hukang@dreamwiz.com
색소녹내장이 동반된 홍채각막내피증후군 1예
김지연1,강자헌2
Department of Ophthalmology, Chonbuk National University College of Medicine1, Cheonbuk, Korea Department of Ophthalmology, Kyunghee University East-West Neo Medical Center2, Seoul, Korea
Correspondence:  Ji Yeon Kim, M.D.1
Abstract
PURPOSE
To report a case of iridocorneal endothelial syndrome with pigmentary glaucoma. METHODS: We encountered a 44-year-old unilateral glaucoma patient who complained of intermittently decreased visual acuity in the right eye. For differential diagnosis, we carried out ophthalmic and systemic examination. RESULTS: Binocular corrected visual acuity was 1.0. His intraocular pressure, measured using a Goldmann applanation tonometer, was 50 mm Hg in the right eye and 18mm Hg in the left. Upon examination of the right eye, we found pigments with a Krukenberg's spindle appearance on the corneal endothelium, peripheral anterior synechia extending beyond Schwalbe's line, trabecular hyperpigmentation, endothelial pleomorphism, polymegathism, cell loss, dark area within the cells, a light central spot and light peripheral zone, retinal nerve fiber layer defects, and visual field defects, which together led to the diagnosis of iridocorneal endothelial syndrome with pigmentary glaucoma. We observed progressed glaucomatous injury upon examination of the disc stereo photograph, retinal nerve fiber layer photograph, and visual field test, even though we used topical IOP reducers. Eventually, we performed a trabeculectomy in the right eye. CONCLUSIONS: We experienced a case of iridocorneal endothelial syndrome with unilateral pigmentary glaucoma. The glaucoma was not well-controlled with topical IOP reducers. The glaucoma was then treated by a trabeculectomy. We report this case with a review of the literature.
Key Words: Iridocorneal endothelial syndrome;Pigmentary glaucoma


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