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Published on: December 22, 2016
Successful outcome of progressive multifocal leukoencephalopathy in a renal transplant patient
Clinton D Crowder1, Kymberly A Gyure, Cinthia B Drachenberg
1Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Abstract:
We report the case of a 47-year-old man who developed progressive multifocal leukoencephalopathy (PML) after receiving immuno-suppressive therapy for renal transplantation. The patient presented with a focal seizure and cognitive changes 5 months post-transplantation. He was found to have enhancing lesions in the parietal lobe and typical findings of PML in a brain biopsy. Immunosuppression was discontinued and the neurological symptoms gradually resolved over a period of 4 weeks. The patient is free of any neurological symptoms 36 months after the diagnosis of PML and imaging studies demonstrate resolution of the PML lesions. The patient returned to hemodialysis 3 months after immunosuppression was discontinued. We also present a review of the literature on PML in renal transplant recipients.
Insights
A 47-year-old man recovered from progressive multifocal leukoencephalopathy (PML) after immunosuppressive therapy for a kidney transplant. Discontinuing immunosuppression led to symptom resolution and lesion clearance, highlighting PML
Area of Science:
- Neuroimmunology
- Nephrology
- Infectious Diseases
Background:
- Renal transplantation requires immunosuppressive therapy to prevent organ rejection.
- Immunosuppression can increase the risk of opportunistic infections, including viral encephalitis.
- Progressive multifocal leukoencephalopathy (PML) is a rare, demyelinating disease of the central nervous system.
Observation:
- A 47-year-old male renal transplant recipient developed focal seizures and cognitive decline 5 months post-transplantation.
- Brain biopsy confirmed findings consistent with progressive multifocal leukoencephalopathy (PML).
- The patient exhibited enhancing lesions in the parietal lobe.
Findings:
- Discontinuation of immunosuppressive therapy resulted in gradual neurological symptom resolution over 4 weeks.
- Follow-up imaging 36 months post-diagnosis showed complete resolution of PML lesions.
- The patient returned to hemodialysis 3 months after stopping immunosuppression.
Implications:
- Early recognition and management of PML in renal transplant recipients are crucial.
- Reversal of immunosuppression can lead to favorable outcomes in PML cases.
- This case underscores the importance of monitoring for opportunistic infections post-transplantation.
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