POST-TRANSPLANT ACUTE LIMBIC ENCEPHALITIS: CLINICAL FEATURES AND RELATIONSHIP TO HHV6
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To the Editor:
Seeley and colleagues present a case control series of nine patients with post-transplant acute limbic encephalitis (PALE) due to presumed reactivation of the human herpes 6 virus (HHV6).1 We present a case of HHV6 encephalitis that clinically presented as a nonspecific encephalopathy that without appropriate CSF assay would have been overlooked and misdiagnosed.
A 55-year-old woman with refractory diffuse large cell non-Hodgkin lymphoma was treated with high-dose chemotherapy and an unmatched allogenic stem cell transplantation. At week 2, she developed post-transplant graft-versus-host disease (bowel and lungs) managed with oral steroids, tacrolimus, and cyclosporine. Three weeks post-transplant, she developed a slowly progressive confusional state.
Routine laboratory evaluation was unremarkable except for neutropenia (530 cells/uL) and thrombocytopenia (38,000 cells/uL). CT and MR imaging of the brain were normal on two occasions over the course of 10 days. EEG revealed mild diffuse generalized slowing in the 6- to 7-Hz range without epileptiform abnormalities. CSF analysis revealed a white blood cell count of 10 cells/mm3 (all lymphocytes), 1 red blood cell/mm3, glucose 87 mg/dL, and protein 80 mg/dL. Viral, bacterial, and fungal cultures were negative. However, HHV6 was positive by quantitative PCR assay in both blood and CSF. The patient was treated with intravenous ganciclovir and foscarnet and made a complete recovery at discharge.
HHV6 exhibits neurotropism and is a rare cause of encephalitis predominantly seen in immunocompromised and occasionally immunocompetent patients.1–5 Features of a limbic encephalitis with characteristic MRI have been reported …
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