Pediatric Neurology
Volume 43, Issue 1 , Pages 53-56, July 2010

High-Dose Ganciclovir in HHV-6 Encephalitis of an Immunocompetent Child

  • Tuire Olli-Lähdesmäki, MD

      Affiliations

    • Department of Pediatrics and Pediatric Neurology, Turku University Hospital, Turku, Finland
    • Corresponding Author InformationCommunications should be addressed to: Dr. Olli-Lähdesmäki; Department of Pediatrics and Pediatric Neurology; Turku University Hospital; Kiinamyllynkatu 4-8; FIN-20520 Turku, Finland.
  • ,
  • Leena Haataja, MD

      Affiliations

    • Department of Pediatrics and Pediatric Neurology, Turku University Hospital, Turku, Finland
  • ,
  • Riitta Parkkola, MD

      Affiliations

    • Department of Radiology, Turku University Hospital, Turku, Finland
  • ,
  • Matti Waris, PhD

      Affiliations

    • Department of Virology, Turku University, Turku, Finland
  • ,
  • Nathalie Bleyzac, MD

      Affiliations

    • Pharmacy Department, Debrousse Hospital, Lyon, France
  • ,
  • Olli Ruuskanen, MD

      Affiliations

    • Department of Pediatrics and Pediatric Neurology, Turku University Hospital, Turku, Finland

Received 28 September 2009; accepted 22 February 2010.

Encephalitis and other neurologic complications, including acute necrotizing encephalopathy, are associated with human herpesvirus-6 infection. Antiviral treatment against human herpesvirus-6 infection is indicated only for immunocompromised patients. We describe a 15-month-old immunocompetent child with severe human herpesvirus-6-induced encephalitis. The primary infection was characterized by human herpesvirus-6 DNA in cerebrospinal fluid and serum, the presence of serum human herpesvirus-6 immunoglobulin M antibodies, and a rise in serum human herpesvirus-6 immunoglobulin G antibodies. Magnetic resonance imaging demonstrated multiple, partly symmetric, necrotic lesions in the pons, medulla oblongata, thalamus, external capsules, and occipital subcortical and cortical areas. High-dose ganciclovir (18 mg/kg/day) was used as antiviral treatment, without side effects. A pharmacokinetic analysis of ganciclovir was performed. The initial recovery from severe disease was good. At 3-year follow-up, neurologic sequelae included epilepsy and ataxia. This case suggests that treatment with ganciclovir should be considered in human herpesvirus-6 central nervous system infections because the neurologic sequelae may otherwise be severe. Controlled, prospective, clinical trials are warranted, to analyze the pharmacokinetics of ganciclovir in infants.

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PII: S0887-8994(10)00083-4

doi:10.1016/j.pediatrneurol.2010.02.003

Pediatric Neurology
Volume 43, Issue 1 , Pages 53-56, July 2010