학술논문

Next-generation sequencing of a large uveal melanoma with whole genome doubling and a PBRM1 mutation
Document Type
article
Source
Subject
Biomedical and Clinical Sciences
Ophthalmology and Optometry
Rare Diseases
Cancer
Clinical Research
Biotechnology
Eye Disease and Disorders of Vision
Genetics
Human Genome
Cancer Genomics
Choroidal melanoma
Melanomalytic glaucoma
Next-generation sequencing
Uveal melanoma
Language
Abstract
PurposeTo report a large uveal melanoma with extra-scleral extension which underwent spontaneous infarction and its unique molecular signature profile.ObservationsAn 81-year-old female presented with a blind, painful eye. Intraocular pressure was 48 mm Hg. There was a large subconjunctival melanotic mass overlying a choroidal melanoma with anterior extension involving the ciliary body and the iridocorneal angle and iris. Ultrasonography confirmed a dome-shaped anterior cilio-choroidal mass with extra-scleral extension. The patient underwent enucleation and pathologic evaluation confirmed cilio-choroidal melanoma. The posterior half of the tumor involving the ciliary body and the extra-scleral component were spontaneously infarcted and were composed of large melanophages. Next-generation sequencing demonstrated a splice site mutation in PBRM1 and whole-genome doubling in addition to a GNAQ hotspot mutation, chromosome 3 loss and 8q gain.Conclusions and importanceThis case of a large, auto-infarcted uveal melanoma demonstrates a PBRM1 mutation and whole-genome doubling.