How we diagnose and treat vitreoretinal lymphoma.

@article{Fend2016HowWD,
  title={How we diagnose and treat vitreoretinal lymphoma.},
  author={Falko Fend and Andr{\'e}s J M Ferreri and Sarah E Coupland},
  journal={British journal of haematology},
  year={2016},
  volume={173 5},
  pages={680-92}
}
The eye is a rare site for the development of malignant lymphoma. Based on cell type and involved intraocular structures, which as a whole represent an immune-privileged site, several subtypes of primary intraocular lymphoma need to be discerned. Primary vitreoretinal lymphoma (PVRL), the most common form, is an aggressive B-cell malignancy and considered a subtype of primary central nervous system (CNS) lymphoma. Ocular symptoms are non-specific and often mimic uveitis, frequently resulting in… CONTINUE READING
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