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Acyclovir resistance in herpes simplex virus type I encephalitis: a case report
Acyclovir resistance is rarely seen in herpes simplex virus (HSV) type I encephalitis. Prevalence rates vary between 0.5 % in immunocompetent patients (Christophers et al. 1998; Fife et al. 1994) and 3.5–10 % in immunocompromised patients (Stranska et al. 2005). We report a 45-year-old, immunocompet...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477561/ https://www.ncbi.nlm.nih.gov/pubmed/27787806 http://dx.doi.org/10.1007/s13365-016-0489-5 |
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author | Bergmann, M. Beer, R. Kofler, M. Helbok, R. Pfausler, B. Schmutzhard, E. |
author_facet | Bergmann, M. Beer, R. Kofler, M. Helbok, R. Pfausler, B. Schmutzhard, E. |
author_sort | Bergmann, M. |
collection | PubMed |
description | Acyclovir resistance is rarely seen in herpes simplex virus (HSV) type I encephalitis. Prevalence rates vary between 0.5 % in immunocompetent patients (Christophers et al. 1998; Fife et al. 1994) and 3.5–10 % in immunocompromised patients (Stranska et al. 2005). We report a 45-year-old, immunocompetent (negative HIV antigen/antibody testing), female patient, without previous illness who developed—after a febrile prodromal stage—aphasia and psychomotor slowing. Cerebral magnetic resonance imaging (cMRI) showed right temporal and insular T2-hyperintense lesions with spreading to the contralateral temporal lobe. Cerebrospinal fluid (CSF) analysis yielded lymphocytic pleocytosis and elevated protein level. Polymerase chain reaction testing for HSV type I showed a positive result in repeat lumbar puncture. HSV type I encephalitis was diagnosed and intravenous acyclovir treatment was initiated (750 mg t.i.d.). Acyclovir treatment was intensified to 1000 mg t.i.d., due to clinical deterioration, ongoing pleocytosis and progression on cMRI 5 days after initiation of antiviral therapy. In parallel, acyclovir resistance testing showed mutation of thymidine kinase gene at position A156V prompting foscarnet therapy (60 mg t.i.d.). Patient’s condition improved dramatically over 2 weeks. Acyclovir resistance is rare but should be considered in case of clinical worsening of patient’s condition. To our knowledge, this is the first report of acyclovir resistance in HSV type I encephalitis of an immunocompetent and previously healthy patient in Austria. |
format | Online Article Text |
id | pubmed-5477561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-54775612017-07-13 Acyclovir resistance in herpes simplex virus type I encephalitis: a case report Bergmann, M. Beer, R. Kofler, M. Helbok, R. Pfausler, B. Schmutzhard, E. J Neurovirol Case Report Acyclovir resistance is rarely seen in herpes simplex virus (HSV) type I encephalitis. Prevalence rates vary between 0.5 % in immunocompetent patients (Christophers et al. 1998; Fife et al. 1994) and 3.5–10 % in immunocompromised patients (Stranska et al. 2005). We report a 45-year-old, immunocompetent (negative HIV antigen/antibody testing), female patient, without previous illness who developed—after a febrile prodromal stage—aphasia and psychomotor slowing. Cerebral magnetic resonance imaging (cMRI) showed right temporal and insular T2-hyperintense lesions with spreading to the contralateral temporal lobe. Cerebrospinal fluid (CSF) analysis yielded lymphocytic pleocytosis and elevated protein level. Polymerase chain reaction testing for HSV type I showed a positive result in repeat lumbar puncture. HSV type I encephalitis was diagnosed and intravenous acyclovir treatment was initiated (750 mg t.i.d.). Acyclovir treatment was intensified to 1000 mg t.i.d., due to clinical deterioration, ongoing pleocytosis and progression on cMRI 5 days after initiation of antiviral therapy. In parallel, acyclovir resistance testing showed mutation of thymidine kinase gene at position A156V prompting foscarnet therapy (60 mg t.i.d.). Patient’s condition improved dramatically over 2 weeks. Acyclovir resistance is rare but should be considered in case of clinical worsening of patient’s condition. To our knowledge, this is the first report of acyclovir resistance in HSV type I encephalitis of an immunocompetent and previously healthy patient in Austria. Springer International Publishing 2016-10-27 2017 /pmc/articles/PMC5477561/ /pubmed/27787806 http://dx.doi.org/10.1007/s13365-016-0489-5 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Case Report Bergmann, M. Beer, R. Kofler, M. Helbok, R. Pfausler, B. Schmutzhard, E. Acyclovir resistance in herpes simplex virus type I encephalitis: a case report |
title | Acyclovir resistance in herpes simplex virus type I encephalitis: a
case report |
title_full | Acyclovir resistance in herpes simplex virus type I encephalitis: a
case report |
title_fullStr | Acyclovir resistance in herpes simplex virus type I encephalitis: a
case report |
title_full_unstemmed | Acyclovir resistance in herpes simplex virus type I encephalitis: a
case report |
title_short | Acyclovir resistance in herpes simplex virus type I encephalitis: a
case report |
title_sort | acyclovir resistance in herpes simplex virus type i encephalitis: a
case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477561/ https://www.ncbi.nlm.nih.gov/pubmed/27787806 http://dx.doi.org/10.1007/s13365-016-0489-5 |
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