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Updated: May 3, 2026

Murine Bilateral Renal Lymphadenectomy
Published on: December 30, 2025
Primary brain lymphomas after kidney transplantation: an under-recognized problem?
Nuria Sola-Valls1, Néstor Yesid Rodríguez C, Carola Arcal
1Hospital Clinic, Barcelona, Catalonia, Spain.
Primary central nervous system post-transplant lymphoproliferative disease (CNS PTLD) is a challenging complication. Early diagnosis and aggressive screening are crucial for managing this rare but serious condition in transplant patients.
Area of Science:
- Neuroscience
- Immunology
- Oncology
Background:
- Primary central nervous system post-transplant lymphoproliferative disease (CNS PTLD) is a rare but severe complication following solid organ transplantation.
- The incidence of CNS PTLD may increase with the use of novel biological agents in immunosuppression protocols.
Purpose of the Study:
- To investigate the clinical characteristics, diagnosis, and outcomes of CNS PTLD in transplant recipients.
- To highlight the diagnostic challenges and emphasize the need for early detection.
Main Methods:
- Retrospective analysis of five cases of CNS PTLD diagnosed between 1986 and 2007.
- Review of clinical presentation, diagnostic workup including serology, in situ hybridization, and PCR for Epstein-Barr virus (EBV), and treatment outcomes.
Main Results:
- The mean time from transplantation to neurological symptoms was over 6 years, with diagnosis taking an average of 3.5 months.
- Clinical manifestations were diverse, including headache, gait disturbance, and confusion. EBV was detected in most cases via serology, biopsy, or CSF PCR.
- Treatment involved reducing immunosuppression, but mortality remained high, with three of four treated patients dying within 2 years.
Conclusions:
- CNS PTLD is difficult to diagnose, often detected late, and frequently resistant to treatment.
- A proactive screening approach is recommended for transplant patients presenting with even subtle central nervous system symptoms.
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