Ischemic Stroke due to Virologically-Confirmed Varicella Zoster Virus Vasculopathy: A Case Series.


Journal

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
ISSN: 1532-8511
Titre abrégé: J Stroke Cerebrovasc Dis
Pays: United States
ID NLM: 9111633

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 28 07 2018
revised: 26 09 2018
accepted: 01 10 2018
pubmed: 6 11 2018
medline: 29 1 2019
entrez: 6 11 2018
Statut: ppublish

Résumé

Limited data are available regarding the characteristics and prognosis of patients with stroke due to varicella zoster virus (VZV) vasculopathy. We studied 4 patients (2 men and 2 women; age, 38-63 years) from a single center who developed acute ischemic stroke due to VZV vasculopathy. The virological diagnosis was confirmed by detecting VZV DNA and/or the IgG antibody to VZV in the cerebrospinal fluid. Three patients were taking immunosuppressive agents, including prednisolone and/or methotrexate, at baseline. Each patient had a characteristic skin rash prior to stroke, with the interval from rash to stroke onset ranging from 13 to 122 days. Two patients experienced antecedent cranial nerve palsies; one had the third, seventh, ninth, and 10th nerve palsies and the other had the fourth nerve palsy before stroke. Cerebral infarctions were located in the anterior circulation lesion (n = 1), in the posterior circulation lesion (n = 2), and in both lesions (n = 1). Intracranial arterial stenosis was only identified in one patient on magnetic resonance angiography. A high plasma d-dimer level was detected in 1 patient, whereas high β-thromboglobulin and platelet factor 4 levels were detected in 2 patients. As a result of combined therapies with acyclovir, steroid, and antithrombotic agents, neurological symptoms markedly improved in 3 patients, whereas 1 patient was left with moderate hemiplegia. Cranial nerve palsies may be prodromal symptoms of VZV-associated stroke. Increased levels of thrombotic markers may support the use of antithrombotic agents, although the benefit of combined treatment should be determined through larger studies.

Sections du résumé

BACKGROUND BACKGROUND
Limited data are available regarding the characteristics and prognosis of patients with stroke due to varicella zoster virus (VZV) vasculopathy.
METHODS METHODS
We studied 4 patients (2 men and 2 women; age, 38-63 years) from a single center who developed acute ischemic stroke due to VZV vasculopathy. The virological diagnosis was confirmed by detecting VZV DNA and/or the IgG antibody to VZV in the cerebrospinal fluid.
RESULTS RESULTS
Three patients were taking immunosuppressive agents, including prednisolone and/or methotrexate, at baseline. Each patient had a characteristic skin rash prior to stroke, with the interval from rash to stroke onset ranging from 13 to 122 days. Two patients experienced antecedent cranial nerve palsies; one had the third, seventh, ninth, and 10th nerve palsies and the other had the fourth nerve palsy before stroke. Cerebral infarctions were located in the anterior circulation lesion (n = 1), in the posterior circulation lesion (n = 2), and in both lesions (n = 1). Intracranial arterial stenosis was only identified in one patient on magnetic resonance angiography. A high plasma d-dimer level was detected in 1 patient, whereas high β-thromboglobulin and platelet factor 4 levels were detected in 2 patients. As a result of combined therapies with acyclovir, steroid, and antithrombotic agents, neurological symptoms markedly improved in 3 patients, whereas 1 patient was left with moderate hemiplegia.
CONCLUSIONS CONCLUSIONS
Cranial nerve palsies may be prodromal symptoms of VZV-associated stroke. Increased levels of thrombotic markers may support the use of antithrombotic agents, although the benefit of combined treatment should be determined through larger studies.

Identifiants

pubmed: 30392831
pii: S1052-3057(18)30580-9
doi: 10.1016/j.jstrokecerebrovasdis.2018.10.001
pii:
doi:

Substances chimiques

Antiviral Agents 0
Fibrinolytic Agents 0
Steroids 0
Acyclovir X4HES1O11F

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

338-343

Informations de copyright

Copyright © 2018 National Stroke Association. Published by Elsevier Inc. All rights reserved.

Auteurs

Takao Hoshino (T)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: hoshino.takao@twmu.ac.jp.

Sono Toi (S)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: toi.sono@twmu.ac.jp.

Kunio Toda (K)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: joykunio@yahoo.co.jp.

Yumiko Uchiyama (Y)

Department of Neurology, Tokyo Women's Medical University Yachiyo Medical Center, Chiba, Japan. Electronic address: yyyy@nij.twmu.ac.jp.

Hiroshi Yoshizawa (H)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: hyoshizaw@nij.twmu.ac.jp.

Mutsumi Iijima (M)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: iijima.mutsumi@twmu.ac.jp.

Yuko Shimizu (Y)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: yshimizu@nij.twmu.ac.jp.

Kazuo Kitagawa (K)

Department of Neurology, Tokyo Women's Medical University Hospital, Tokyo, Japan. Electronic address: kitagawa.kazuo@twmu.ac.jp.

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