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Published in: Child's Nervous System 11/2007

01-11-2007 | Case Report

HSV encephalitis in a child with brain stem glioma: a rare complication of therapy

Case report and review of the neurosurgical literature

Authors: Barbara Spacca, Conor Mallucci, Andrew Riordan, Richard Appleton, Nicky Thorp, Barry Pizer

Published in: Child's Nervous System | Issue 11/2007

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Abstract

Background

Herpes simplex virus (HSV) encephalitis is a rare association with pediatric neurosurgical pathologies.

Case report

A 13-year-old boy was diagnosed with an inoperable, biopsy-proven pontine grade II astrocytoma. During radiotherapy, he developed status epilepticus controlled by thiopentone with intubation and ventilation. Empiric cefotaxime and aciclovir were given. Lumbar cerebrospinal fluid (CSF) showed a normal white cell count, normal glucose, and a slightly elevated protein level. However, the CSF showed a positive polymerase chain reaction (PCR) for HSV type 1 DNA. Intravenous aciclovir was given for 21 days and foscarnet for 7 days. He was extubated after 4 weeks at which time he was aphasic with spastic diplegia. After 8 weeks, MRI brain scan showed the typical bitemporal pattern of HSV encephalitis. He made slow improvement but died 8 months after diagnosis from tumor progression.

Conclusion

HSV encephalitis is a rare but life threatening complication in neurosurgical patients. A low threshold for both investigation with CSF PCR and empirical treatment with intravenous aciclovir is warranted. As in this case, initial microscopic examination of the CSF may be normal. The literature on HSV encephalitis in neurosurgical patients is discussed.
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Metadata
Title
HSV encephalitis in a child with brain stem glioma: a rare complication of therapy
Case report and review of the neurosurgical literature
Authors
Barbara Spacca
Conor Mallucci
Andrew Riordan
Richard Appleton
Nicky Thorp
Barry Pizer
Publication date
01-11-2007
Publisher
Springer-Verlag
Published in
Child's Nervous System / Issue 11/2007
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-007-0389-3

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