Multifocal Congenital Simple Hamartoma of the Retinal Pigment Epithelium: A Multimodal Imaging Case Study

被引:1
|
作者
Khadamy, Joobin [1 ,2 ]
Sadr, Navid Elmi [3 ,4 ]
机构
[1] Skelleftea Eye Clin, Ophthalmol, Skelleftea, Sweden
[2] Univ Hosp Umea, Ophthalmol, Umea, Sweden
[3] Semnan Univ Med Sci, Ophthalmol, Semnan, Iran
[4] Semnan Univ Med Sci, Kowsar Educ Res & Therapeut Hosp, Clin Res Dev Unit, Semnan, Iran
关键词
choroidal malignant melanoma; chrpe (congenital hypertrophy of the retinal pigment epithelium); oct (optical coherence tomography); retinal pigment lesion; indocyanine green angiography; fluorescein angiography; optical coherence tomography; multimodal imaging; cshrpe; congenital simple hamartoma of the retinal pigment epithelium;
D O I
10.7759/cureus.60755
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital simple hamartoma of the retinal pigment epithelium (CSHRPE) is a rare benign tumor often detected incidentally during routine eye exams. We present a case of multifocal CSHRPE in a 32-year-old Hispanic woman, emphasizing the diagnostic challenges posed by its presentation and the pivotal role of multimodal imaging in accurate diagnosis. Despite initial difficulties due to a history of trauma and pigmented fundus, advanced imaging techniques, including optical coherence tomography (OCT), OCT angiography (OCTA), fluorescein angiography (FA), and indocyanine green angiography (ICGA), facilitated a precise diagnosis. Notably, OCTA revealed high signal intensity and flow at the largest nodule site while FA and ICGA exhibited characteristic blockage patterns. Moreover, smaller nodules exhibited OCT findings supporting the theory of islands of retinal pigment epithelium (RPE) cells proliferating ectopically within the retina. Our case underscores the importance of comprehensive imaging assessment in distinguishing CSHRPE from other lesions, contributing to a deeper understanding of this rare ocular condition.
引用
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页数:8
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