Abstract
Status epilepticus after allogeneic hematopoietic cell transplantation (alloHCT) is rare. The authors report a case involving a 65-year-old man with nonconvulsive status epilepticus 34 days after umbilical cord blood transplantion for chronic lymphocytic leukemia. Cerebrospinal fluid and serum were positive for human herpesvirus 6 (HHV6). Magnetic resonance imaging of the brain showed symmetric T2 hyperintensity bilaterally in the mesial temporal lobes, and T2 hyperintensities and restricted diffusion of bilateral putamina. Despite aggressive anticonvulsive therapy, his seizures only abated with initiation of ganciclovir therapy. The patient completed six weeks of combination antiviral therapy (ganciclovir and foscarnet). His cognitive function gradually improved and, after prolonged rehabilitation, the patient was discharged home with residual intermittent memory loss but otherwise functional. HHV6 should be considered in the differential diagnosis of nonconvulsive status epilepticus after alloHCT, especially in patients with hyponatremia. Empirical antiviral therapy targeting HHV6 should be administered to these patients.
Original language | English (US) |
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Pages (from-to) | 170-172 |
Number of pages | 3 |
Journal | Canadian Journal of Infectious Diseases and Medical Microbiology |
Volume | 25 |
Issue number | 3 |
DOIs | |
State | Published - 2014 |
Keywords
- Human herpesvirus 6
- Hyponatremia
- Immunocompromised host
- Status epilepticus
- Umbilical cord blood transplantation