Primary central nervous system lymphoma—current standards and recent developments
Abstract Primary central nervous system lymphoma (PCNSL) is a rare aggressive B-cell non-Hodgkin lymphoma confined to the central nervous system, without systemic involvement. The incidence has increased over the past 3 decades. The prognosis has improved in patients up to 70 years old, and this type of lymphoma can be potentially cured. The gold standard of diagnosing PCNSL is histological, usually on a brain biopsy specimen via a neurosurgical procedure. Recent developments in both imaging and laboratory analyses of the cerebrospinal fluid, can be helpful in narrowing the differential diagnosis, diagnosing PCNSL itself, and in follow-up after treatment. This narrative review gives an overview of the epidemiology, diagnosis, and treatment of PCNSL, with an emphasis on recent developments in diagnostic techniques and treatment.
Authors
- Jeanette K. Doorduijn (ORCID: https://orcid.org/0000-0002-1014-0918)
- J. S. Vermaat
- N Galldiks
- Jeroen de Bresser (ORCID: https://orcid.org/0000-0003-0759-8407)
- Samar Issa (ORCID: https://orcid.org/0009-0008-2534-3428)
- Matthijs van der Meulen
- Jacoline E C Bromberg
Institutions
- Forschungszentrum Jülich (DE)
- Leiden University Medical Center (NL)
- Middlemore Hospital (NZ)
- Erasmus MC Cancer Institute (NL)
- University Hospital Cologne (DE)
Publication Details
- Journal
- Neuro-Oncology Practice
- Published
- 2026-02-23
- DOI
- https://doi.org/10.1093/nop/npag016
- Primary Topic
- CNS Lymphoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00