Opalski Syndrome Treated with Intravenous Recombinant Tissue Type Plasminogen Activator-Case Report and Review of Literature.


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:
Aug 2020
Historique:
received: 27 01 2020
revised: 28 02 2020
accepted: 04 03 2020
pubmed: 22 5 2020
medline: 28 10 2020
entrez: 22 5 2020
Statut: ppublish

Résumé

A 65-year-old man with a history of Wallenberg syndrome caused by vertebral artery dissection at 62 years old was admitted to our hospital with nausea, vertigo, right facial dysesthesia, right hemiplegia, crossed sensory disturbance (sensory loss and numbness in the right face and left body below the neck), and right limb ataxia. Magnetic resonance imaging (MRI) performed 80 minutes after onset revealed no acute ischemic stroke lesions, but magnetic resonance angiography (MRA) demonstrated complete occlusion of the right vertebral artery. Based on these neurological and MRA findings, atypical lateral medullary infarction was suggested, and intravenous tissue plasminogen activator (IV-tPA) was started 178 minutes after onset. Right hemiplegia improved immediately after IV-tPA administration. MRI performed on hospital day 2 showed an acute ischemic lesion on the right side of the medulla oblongata, resulting in a diagnosis of Opalski syndrome. Opalski syndrome is a rare subtype of Wallenberg syndrome accompanied by hemiplegia of the side ipsilateral to the lesion, and expansion of the stroke lesion to the corticospinal tract below the pyramidal decussation is considered to cause ipsilateral hemiplegia. Based on this case and previous reports, Opalski syndrome should be considered when limb ataxia and crossed sensory deficit are observed among patients with hyperacute-onset hemiplegia, and IV t-PA therapy should be considered even in the absence of neurological findings such as dysphagia, dysarthria, and Horner's signs and radiological evidence of acute ischemic stroke.

Identifiants

pubmed: 32434729
pii: S1052-3057(20)30190-7
doi: 10.1016/j.jstrokecerebrovasdis.2020.104806
pii:
doi:

Substances chimiques

Fibrinolytic Agents 0
Recombinant Proteins 0
Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

104806

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of Interest None.

Auteurs

Daisuke Hara (D)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan. Electronic address: spw29zq9@marianna-u.ac.jp.

Masashi Akamatsu (M)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

Heisuke Mizukami (H)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

Bunta Kato (B)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

Takaaki Suzuki (T)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

Jun Oshima (J)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

Yukari Akasu (Y)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

Yasuhiro Hasegawa (Y)

Department of Internal Medicine, Division of Neurology, St. Marianna University School of Medicine, Yokohama City Seibu Hospital, Kanagawa, Japan.

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