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Published on: April 28, 2013
Severe parvovirus B19 encephalitis after renal transplantation
M Laurenz1, B Winkelmann, J Roigas
1Department of Pediatric Nephrology, Charité Universitätsmedizin, Berlin, Germany.
Insights
Human parvovirus B19 can cause severe illness in transplant patients. In this case, a kidney transplant recipient developed encephalitis and anemia, likely from the donated organ, and recovered after immunosuppression was reduced.
Area of Science:
- Virology
- Immunology
- Nephrology
Background:
- Human parvovirus B19 commonly causes erythema infectiosum (fifth disease) in children.
- Immunocompromised individuals are susceptible to chronic parvovirus B19 infections, leading to hyporegenerative anemia.
Observation:
- A nine-year-old boy developed seizures and encephalitis post-renal transplantation.
- The patient exhibited anemia, high parvovirus B19 viral load, and seroconversion.
- The donated organ was identified as the likely source of parvovirus B19 infection.
Findings:
- Parvovirus B19 infection was confirmed in a post-renal transplant patient presenting with neurological symptoms.
- High viral loads and anemia were key indicators of active infection.
- Reduction in immunosuppressive therapy led to clinical recovery and normalization of red blood cell count.
Implications:
- Parvovirus B19 should be considered in the differential diagnosis of seizures in solid organ transplant recipients.
- This case highlights the potential for organ transmission of parvovirus B19.
- Management strategies may involve adjusting immunosuppression in transplant patients with parvovirus B19 infection.
Abstract:
Human parvovirus B19 is a common cause of benign erythema infectiosum (fifth disease) in otherwise healthy children. Immunocompromized patients are at risk of developing chronic infections leading to chronic hyporegenerative anemia. We report the case of a nine-year-old boy who presented five days after renal transplantation with seizures and signs of encephalitis on MRI. The clinical course was characterized by anemia and seroconversion for parvovirus B19 accompanied by a high viral load (>10(9) copies per milliliter). A transfusion of red blood cells that the patient required after transplantation was found to be negative for parvovirus B19, leaving the donated organ as the most likely source of infection. Reduction of the immunosuppressive regimen led to complete recovery of the patient with a stable RBC count upon discharge. Parvovirus B19 infections should be considered in the differential diagnosis of seizures after solid organ transplantation.
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