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.

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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