Title of article
Uveal melanoma: Ocular and systemic disease
Author/Authors
Miyamoto, Cristina McGill University Health Center - Henry C Witelson Ocular Pathology Laboratory, Canada , Balazsi, Matthew McGill University Health Center - Henry C Witelson Ocular Pathology Laboratory, Canada , Bakalian, Silvin McGill University Health Center - Henry C Witelson Ocular Pathology Laboratory, Canada , Fernandes, Bruno F. McGill University Health Center - Henry C Witelson Ocular Pathology Laboratory, Canada , Burnier, Miguel N. Jr McGill University Health Center - Henry C Witelson Ocular Pathology Laboratory, Canada
From page
145
To page
149
Abstract
Although rare, uveal melanoma is the most common intraocular tumor in adults. Most cases arise from the choroidal layer of the uvea, displaying a discoid, collar-button, or mushroom shaped growth. Histopathologically, neoplasms are classified by the dominant cell type: spindle, epithelioid or mixed spindle cell type. The most important prognostic factors are cell type, nucleolar size, largest tumor dimension, and mitotic figures. Patient prognosis is poor when metastases occur in the liver, one of the main reasons that despite advances in the diagnosis and treatment of uveal melanoma, the mortality rate has not change significantly since 1973.
Keywords
Uveal melanoma , Cancer , Metastasis , Choroidal
Journal title
Saudi Journal of Ophthalmology
Journal title
Saudi Journal of Ophthalmology
Record number
2678814
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