Uveal melanoma: Ocular and systemic disease
Author(s) -
Cristina Miyamoto,
Matthew Balazsi,
S. Bakalian,
Bruno F. Fernandes,
Miguel N. Burnier
Publication year - 2012
Publication title -
saudi journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.359
H-Index - 25
eISSN - 2542-6680
pISSN - 1319-4534
DOI - 10.1016/j.sjopt.2012.02.010
Subject(s) - medicine , melanoma , uvea , epithelioid cell , disease , ocular melanoma , pathology , dermatology , cancer research , immunohistochemistry
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.
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