Context: The detection of monosomy 3 in uveal melanomas has repeatedly been associated with adverse outcome. Fine-needle aspiration biopsy is being used to detect monosomy 3 in these tumors, based on the assumption that this chromosomal abnormality is distributed homogeneously throughout the tumor.
Objective: To study the distribution of monosomy 3 in primary uveal melanoma by fluorescence in situ hybridization (FISH).