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Updated: May 18, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Posterior reversible encephalopathy syndrome: the importance of early diagnosis
Rute Teotónio1, Dina Marmoto, Cristina Januário
1Department of Neurology, Hospitais da Universidade de Coimbra, Coimbra, Portugal. rute.teotonio@gmail.com
Insights
Tacrolimus, an immunosuppressant, can cause posterior reversible encephalopathy syndrome (PRES) in young heart transplant patients. Stopping the drug led to clinical and MRI recovery, highlighting the importance of prompt diagnosis.
Area of Science:
- Neurology
- Immunology
- Cardiology
Background:
- Dilated cardiomyopathy necessitates cardiac transplantation in pediatric patients.
- Immunosuppression therapy is critical post-transplant, commonly involving corticosteroids, mycophenolate mofetil, and tacrolimus.
Observation:
- A 14-year-old boy developed focal seizures and drowsiness on day four of immunosuppression post-cardiac transplant.
- Neurological examination revealed right focal seizures and drowsiness, with EEG showing right occipital seizure onset.
- MRI demonstrated diffuse subcortical white matter lesions consistent with vasogenic edema, predominantly in the right hemisphere.
Findings:
- Tacrolimus was identified as the likely cause of posterior reversible encephalopathy syndrome (PRES).
- Discontinuation of tacrolimus resulted in the regression of MRI abnormalities and complete clinical recovery.
- Laboratory and CSF analyses were unremarkable, and drug levels were non-toxic, ruling out other common causes.
Implications:
- Posterior reversible encephalopathy syndrome (PRES) is a rare but serious complication of tacrolimus in solid organ transplant recipients.
- Early recognition and management of tacrolimus-induced PRES are crucial to prevent irreversible neurological damage.
- This case underscores the need for vigilant neurological monitoring in patients receiving tacrolimus-based immunosuppression.
Abstract:
A 14-year-old boy was submitted to cardiac transplant due to a dilated cardiomyopathy. On the fourth day of immunosuppression (corticosteroids, mycophenolate mofetil and tacrolimus), he developed right focal seizures and drowsiness. Blood pressure was in the normal range and laboratory findings in cerebral spinal fluid and blood were unremarkable, with drugs in non-toxic levels. The EEG showed a slow background rhythm more pronounced on the right and a seizure onset in the right occipital region. MRI revealed a diffuse hyperintense subcortical white-matter lesion on fluid attenuated inversion recovery, with lesser involvement of left temporal-occipital region. There was no enhancement with gadolinium and MRI diffusion-weighted imaging was consistent with vasogenic oedema. Tacrolimus was stopped with regression of MRI abnormalities and clinical recovery. Posterior reversible encephalopathy associated with tacrolimus is a rare but potentially serious complication of solid organ transplants. A prompt diagnosis and correct treatment is essential to avoid irreversible brain damage.
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