Isolated Cilioretinal Artery Occlusion in Pseudoexfoliation Syndrome: A Case Report. |
Min Joung Lee, Yeoung Geol Park, Jae Kyoun Ahn |
1Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Korea. 2Seoul Artificial Eye Center, Clinical Research Institute, Seoul National University Hospital, Seoul, Korea. 3Department of Ophthalmology, Chonnam National University Medical School & Hospital, Gwangju, Korea. jkahn@jnu.ac.kr |
거짓비늘증후군에 동반된 단독 섬모체망막동맥폐쇄 1예 |
이민정1,2,박영걸3,안재균3 |
Department of Ophthalmology, Seoul National University College of Medicine1, Seoul, Korea Seoul Artificial Eye Center, Clinical Research Institute, Seoul National University Hospital2, Seoul, Korea Department of Ophthalmology, Chonnam National University Medical School & Hospital3, Gwangju, Korea |
Correspondence:
Min Joung Lee, M.D.1,2 |
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Abstract |
PURPOSE To report a case of isolated cilioretinal artery occlusion associated with pseudoexfoliation syndrome. METHODS: A 66-year-old female presented with acute vision loss of the right eye. Three months prior, she had been diagnosed as having pseudoexfoliation glaucoma of both eyes, and the intraocular pressure of both eyes had been well-controlled with topical medication. RESULTS: The presenting visual acuity in her right eye was 20/100. Fundus examinations showed sectoral retinal whitening on superior macula. Fluorescein angiography revealed delayed filling of the cilioretinal artery, consistent with cilioretinal artery occlusion. No significant findings were identified by carotid doppler examination or echocardiography. After 8 weeks, retinal changes were completely resolved with improvement of her right vision to 20/25. CONCLUSIONS: Isolated cilioretinal artery occlusion may develop as an intraocular manifestation of pseudoexfoliation syndrome. |
Key Words:
Cilioretinal artery occlusion;Ischemia;Pseudoexfoliation syndrome |
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