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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.
Unlabelled:
Primary central nervous system post-transplant lymphoproliferative disease (CNS PTLD) is a serious complication after solid organ transplantation that has not received much attention so far. However, it could become a more frequent problem with the introduction of new biological agents.
Methods:
We identified five cases with CNS PTLD in our center who were transplanted between 1986 and 2007, three men and two women, with a mean age of 55.9 years (range 42-74). Three patients had received only kidney transplant and two patients had received a kidney-pancreas transplant.
Results:
The mean time from first symptoms until diagnosis was 3.5 months (2-6). One patient was diagnosed post-mortem in autopsy. The mean time from transplantation to onset of neurological symptoms was 73.8 months (31-144). The initial clinical manifestation was heterogeneous: all five cases showed headache, four cases presented with gait disturbance, one with dysarthria and two with a confusional state. Epstein-Barr virus (EBV) immunoglobulin (Ig)G serology was positive in four out of five cases; in situ hybridization for EBV in brain biopsy samples was positive in three cases, negative in one and not available in one. In four patients, EBV polymerase chain reaction (PCR) was positive in cerebrospinal fluid (CSF). After diagnosis, overall immunosuppressive load was lowered in all patients (n = 4). Three patients died at 8-104 weeks (mean 40 weeks) after diagnosis and one patient is still alive 20 months after diagnosis.
Conclusions:
CNS PTLD is a complication difficult to diagnose, frequently diagnosed too late and often refractory to treatment. A more aggressive screening might be necessary in patients even with mild CNS symptoms.
Insights
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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