2019, Number 4
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Rev Cub Oftal 2019; 32 (4)
Uveal melanoma of ciliary body
Garduño-Vieyra L, Ruiz-Quintero NC, de la Fuente-Batta I
Language: Spanish
References: 10
Page: 1-6
PDF size: 410.28 Kb.
ABSTRACT
The objective of this case report is to describe the characteristics of a conjunctival bulging
nevus in a 72-year-old female patient and the complementary tests that were performed to reach the diagnosis of conjunctival melanoma. Conjunctival melanoma is a rare tumor, which
account for 2% of all eye tumors. The cells involved are the melanocytes of the conjunctival
epithelium. A risk factor for this entity may be exposure to ultraviolet light. However, it has
not been precisely described. Most cases originate from a primary acquired melanosis (50-
70%). The most common presentation is a pigmented, unilateral, elevated, thick, lesion with
blood vessels and areas of melanosis around it. Its diagnosis is made with the clinical suspicion
confirmed with the histopathological study. Current treatment is local excision, followed by
cryotherapy, radiotherapy, or chemotherapy. Metastatic disease occurs in 11-42% and 20-52%
of patients in a 5-year and 10-year follow-up, respectively.
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