Solitary congenital hypertrophy of the retinal pigment epithelium: A case report

Ahmed Ghazza; Achibane Aimrane; Sarah Belghmaidi; Ibtisssam Hajji; Abdeljalil Moutaouakil

doi:10.33545/26648547.2019.v1.i1a.4

Solitary congenital hypertrophy of the retinal pigment epithelium: A case report

Author(s):

Ahmed Ghazza, Achibane Aimrane, Sarah Belghmaidi, Ibtisssam Hajji, Abdeljalil Moutaouakil

Abstract:

Congenital hypertrophy of the retinal pigment epithelium (CHRPE) is a benign pigmented lesion located at the retinal pigment epithelium (1-4). Hyper pigmented fundus lesions are divided into three different forms: solitary, grouped and multiple (5). The solitary form often appears as a flattened pigment spot, generally considered to be benign, with no potential for malignant growth or transformation (6).

DOI: 10.33545/26648547.2019.v1.i1a.4

Pages: 16-17 | 1340 Views 431 Downloads

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How to cite this article:

Ahmed Ghazza, Achibane Aimrane, Sarah Belghmaidi, Ibtisssam Hajji, Abdeljalil Moutaouakil. Solitary congenital hypertrophy of the retinal pigment epithelium: A case report. Int. J. Ophthalmol. Optometry 2019;1(1):16-17. DOI: 10.33545/26648547.2019.v1.i1a.4

Vol. 1, Issue 1, Part A (2019)

Solitary congenital hypertrophy of the retinal pigment epithelium: A case report

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