Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings
Congenital simple hamartoma of retinal pigment epithelium (CSHRPE) is a rare, asymptomatic, and incidentally detected benign lesion. However, it is very important to do the differential diagnosis from other pigmented retinal lesions. Its clinical presentation and imaging findings are very helpful in...
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doaj-d74cbd424e894432a51bd1456473f5462020-11-24T23:46:55ZengHindawi LimitedCase Reports in Ophthalmological Medicine2090-67222090-67302012-01-01201210.1155/2012/654502654502Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging FindingsMehmet Yasin Teke0Pinar Ç. Özdal1Figen Batioglu2Ufuk Elgin3Faruk Öztürk4Retina Department, Ulucanlar Eye Research and Training Hospital, 06460 Ankara, TurkeyRetina Department, Ulucanlar Eye Research and Training Hospital, 06460 Ankara, TurkeyDepartment of Ophthalmology, Ankara University Medical School, 06460 Ankara, TurkeyRetina Department, Ulucanlar Eye Research and Training Hospital, 06460 Ankara, TurkeyRetina Department, Ulucanlar Eye Research and Training Hospital, 06460 Ankara, TurkeyCongenital simple hamartoma of retinal pigment epithelium (CSHRPE) is a rare, asymptomatic, and incidentally detected benign lesion. However, it is very important to do the differential diagnosis from other pigmented retinal lesions. Its clinical presentation and imaging findings are very helpful in doing this differentiation. This paper presents clinical and imaging findings of a 56-year-old woman with incidentally detected CSHRPE. The lesion was small, heavily pigmented, well circumscribed, and slightly elevated. Optical coherence tomography (OCT) scanning was diagnostic and showed an elevated retina at the site of the lesion, increased optical reflectivity on its inner surface, optical shadowing of deeper structures, and clearly cut tumor margins. Ocular ultrasonography, fluorescein angiography, and fundus autofluorescence imaging which is firstly described in this report did not show any characteristic finding.http://dx.doi.org/10.1155/2012/654502 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mehmet Yasin Teke Pinar Ç. Özdal Figen Batioglu Ufuk Elgin Faruk Öztürk |
spellingShingle |
Mehmet Yasin Teke Pinar Ç. Özdal Figen Batioglu Ufuk Elgin Faruk Öztürk Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings Case Reports in Ophthalmological Medicine |
author_facet |
Mehmet Yasin Teke Pinar Ç. Özdal Figen Batioglu Ufuk Elgin Faruk Öztürk |
author_sort |
Mehmet Yasin Teke |
title |
Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings |
title_short |
Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings |
title_full |
Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings |
title_fullStr |
Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings |
title_full_unstemmed |
Congenital Simple Hamartoma of Retinal Pigment Epithelium: Clinical and Imaging Findings |
title_sort |
congenital simple hamartoma of retinal pigment epithelium: clinical and imaging findings |
publisher |
Hindawi Limited |
series |
Case Reports in Ophthalmological Medicine |
issn |
2090-6722 2090-6730 |
publishDate |
2012-01-01 |
description |
Congenital simple hamartoma of retinal pigment epithelium (CSHRPE) is a rare, asymptomatic, and incidentally detected benign lesion. However, it is very important to do the differential diagnosis from other pigmented retinal lesions. Its clinical presentation and imaging findings are very helpful in doing this differentiation. This paper presents clinical and imaging findings of a 56-year-old woman with incidentally detected CSHRPE. The lesion was small, heavily pigmented, well circumscribed, and slightly elevated. Optical coherence tomography (OCT) scanning was diagnostic and showed an elevated retina at the site of the lesion, increased optical reflectivity on its inner surface, optical shadowing of deeper structures, and clearly cut tumor margins. Ocular ultrasonography, fluorescein angiography, and fundus autofluorescence imaging which is firstly described in this report did not show any characteristic finding. |
url |
http://dx.doi.org/10.1155/2012/654502 |
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