Vitreoretinal Lymphoma.
Bianka SobolewskaSoon-Phaik CheeFatma ZaguiaDebra Anne GoldsteinJustine R SmithFalko FendManabu MochizukiManfred ZierhutPublished in: Cancers (2021)
Vitreoretinal lymphoma (VRL) is a rare variant of primary central nervous system lymphoma (PCNSL), mostly of diffuse large B cell lymphoma, which affects the retina and/or the vitreous with or without optic nerve involvement. The disease course is aggressive. Up to 90% of the patients develop central nervous system lymphoma within one year. The diagnosis of VRL is challenging due to nonspecific chronic and relapsing uveitis and is made by anterior chamber tab or vitreous aspirate biopsy. There is no established treatment protocol for VRL patients with bilateral involvement without CNS involvement. There are suggestions to use only intravitreal chemotherapy with methotrexate and/or rituximab. Alternatively, systemic high-dose MTX treatment or external beam radiotherapy is used. Further studies are needed to prove and confirm the prophylactic systemic therapy in preventing CNS involvement in limited VRL.
Keyphrases
- diffuse large b cell lymphoma
- epstein barr virus
- high dose
- optic nerve
- end stage renal disease
- multiple sclerosis
- newly diagnosed
- randomized controlled trial
- blood brain barrier
- stem cells
- ejection fraction
- low dose
- squamous cell carcinoma
- stem cell transplantation
- locally advanced
- peritoneal dialysis
- rheumatoid arthritis
- patient reported outcomes
- bone marrow
- case report
- replacement therapy
- disease activity
- combination therapy
- ultrasound guided
- mesenchymal stem cells
- age related macular degeneration