CASE REPORT
Year : 2016  |  Volume : 24  |  Issue : 1  |  Page : 46-48

Presumed optic disc melanocytoma in a young Nigerian: A diagnostic challenge


Department of Ophthalmology, University College Hospital, University of Ibadan, Ibadan, Nigeria

Correspondence Address:
Dr. Bolutife A Olusanya
Department of Ophthalmology, University College Hospital, University of Ibadan, Ibadan
Nigeria
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0189-9171.179920

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Optic disc melanocytoma (ODM) is a rare, benign, deeply pigmented ocular tumor arising from melanocytes within the optic disc or from any part of the uvea. It occurs more in dark skinned individuals and females. We report a 17-year-old female who presented to our outpatient department with a history of poor distant vision from childhood, worse in the right eye. Ocular examination revealed visual acuity of 6/36 and 6/18 in the right and left eyes, respectively, which improved to 6/9 bilaterally with a pinhole. There was a relative afferent pupillary defect in the right eye, and a posterior segment examination of same eye showed a raised pigmented optic disc lesion occupying the inferior two-thirds of the optic disc and obscuring the lower disc margin. Both the anterior and posterior segments of the left eye were normal. A diagnosis of presumed ODM was made. Spectacles were prescribed, and the patient was counseled on regular follow-up to monitor progression. ODM should be considered in patients presenting with a pigmented optic disc lesion. Regular follow-up with fundus photography is advocated.


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