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Tytuł pozycji:

Extensive VZV Encephalomyelitis without Rash in an Elderly Man.

Tytuł:
Extensive VZV Encephalomyelitis without Rash in an Elderly Man.
Autorzy:
Lynch K; Department of Neurology, Tufts Medical Center, 800 Washington Street, Boston, MA 02111, USA.
Agarwal P; Tufts University School of Medicine, 145 Harrison Avenue, Boston, MA 02111, USA.
Paranandi A; Department of Geographic and Infectious Diseases, Tufts Medical Center, 800 Washington Street, Boston, MA 02111, USA.
Hadley S; Department of Geographic and Infectious Diseases, Tufts Medical Center, 800 Washington Street, Boston, MA 02111, USA.
Vullaganti M; Department of Neurology, Tufts Medical Center, 800 Washington Street, Boston, MA 02111, USA.
Źródło:
Case reports in neurological medicine [Case Rep Neurol Med] 2014; Vol. 2014, pp. 694750. Date of Electronic Publication: 2014 Apr 23.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: New York, NY : Hindawi Pub. Corp.
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Entry Date(s):
Date Created: 20140528 Date Completed: 20140527 Latest Revision: 20211021
Update Code:
20240104
PubMed Central ID:
PMC4017713
DOI:
10.1155/2014/694750
PMID:
24864218
Czasopismo naukowe
Introduction. Varicella zoster virus (VZV) encephalomyelitis with cranial nerve involvement is rare. Characteristically it is preceded by a rash and primarily presents in the immunocompromised. The spectrum of VZV neurologic disease is extensive and it is not uncommon to present without rash. We report the case of an elderly otherwise immunocompetent patient who presented with diverse manifestations of VZV CNS infection all occurring without rash. Case Report. A 78-year-old man presented with 1 week of progressive paraparesis and sensory loss, malaise, and fevers. MRI of the neuraxis demonstrated numerous enhancing lesions: intramedullary, leptomeningeal, pachymeningeal, and cranial nerves. Cerebrospinal fluid (CSF) showed a white blood cell count of 420/ μ L with elevated protein (385 mg/dL). CSF VZV qualitative PCR was positive and CSF VZV immunofluorescence assay detected IgM antibody, confirming the diagnosis of VZV encephalomyelitis. Clinical and radiological improvement was observed after intravenous acyclovir treatment. Conclusion. This is a rare report of an immunocompetent patient with extensive VZV encephalomyelitis. We highlight the importance of considering this diagnosis even in the absence of the characteristic rash, and the potential risk of premature discontinuation of antiviral therapy once HSV has been excluded. Prompt recognition and treatment can dramatically reduce morbidity and mortality in patients.

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