Abstract:
PURPOSE:To report a case of congenital hypertrophy of the retinal pigment epithelium followed up for 7 years showing features not previously reported. METHODS:A complete fundus examination including fluorescein angiography was performed at first examination and at follow-up. RESULTS:The area of congenital hypertrophy of the retinal pigment epithelium presented morphologic changes, showing enlargement of the lesion on one side associated with partial regression on another side. In addition, the indocyanine green angiography findings revealed that this test was more useful than fluorescein angiography to delineate the real boundaries of the lesion and disclosed hypofluorescent areas inside the main lesion that were not appreciated at ophthalmoscopy or fluorescein angiography. CONCLUSIONS:Indocyanine green angiography is an useful test to understand the findings and evolution of congenital hypertrophy of the retinal pigment epithelium.
journal_name
Eur J Ophthalmoljournal_title
European journal of ophthalmologyauthors
Giuffrè Gdoi
10.1177/112067210501500129subject
Has Abstractpub_date
2005-01-01 00:00:00pages
162-4issue
1eissn
1120-6721issn
1724-6016journal_volume
15pub_type
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journal_title:European journal of ophthalmology
pub_type: 杂志文章
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