Mechanical Thrombectomy for Basilar Artery Occlusion with a Type 1 Persistent Proatlantal Artery: A Case Report and Literature Review.

acute ischemic stroke basilar artery occlusion endovascular treatment mechanical thrombectomy persistent proatlantal artery

Journal

Journal of neuroendovascular therapy
ISSN: 2186-2494
Titre abrégé: J Neuroendovasc Ther
Pays: Japan
ID NLM: 101488164

Informations de publication

Date de publication:
2023
Historique:
received: 15 02 2023
accepted: 16 05 2023
medline: 7 8 2023
pubmed: 7 8 2023
entrez: 7 8 2023
Statut: ppublish

Résumé

Persistent proatlantal artery (PPA) is a primitive carotid-vertebrobasilar anastomosis (CVA); acute ischemic stroke due to basilar artery (BA) occlusion via a PPA is extremely rare. An 84-year-old female developed disturbance of consciousness (Glasgow Coma Scale E2V1M5) and quadriparesis with a National Institutes of Health Stroke Scale score of 35. Head CT revealed early ischemic changes in the right temporal lobe, and a hyperdense vessel sign in the BA. Cerebral angiography showed that the left vertebral artery (VA) did not originate from the left subclavian artery or aortic arch. A left common carotid artery angiogram showed the presence of the left PPA originating from the left external carotid artery. Mechanical thrombectomy (MT) with contact aspiration using a Penumbra 5MAX ACE 60 aspiration catheter was performed, and successful recanalization was achieved after clot retrieval in the first attempt (thrombolysis in cerebral infarction scale 2b). MRI performed the following day, however, revealed a newly developed large hemorrhagic infarction in the pons, with no improvement in her symptoms (modified Rankin Scale score of 5 at 90 days). Although MT achieved successful recanalization of the BA via the PPA, her clinical symptoms did not improve, probably because of poor collateral circulation or the long length of the occlusion. In patients with acute vertebro-BA occlusion, if the VA does not originate from the subclavian artery or aortic arch, the presence of a primitive CVA should be considered.

Identifiants

pubmed: 37546343
doi: 10.5797/jnet.cr.2023-0007
pii: jnet.cr.2023-0007
pmc: PMC10400907
doi:

Types de publication

Case Reports

Langues

eng

Pagination

139-144

Informations de copyright

©2023 The Japanese Society for Neuroendovascular Therapy.

Déclaration de conflit d'intérêts

None of the authors have any conflicts of interest in relation to this article.

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Auteurs

Shohei Ito (S)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.

Takumi Asai (T)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.
Department of Neurosurgery, Kariya Toyota General Hospital, Kariya, Aichi, Japan.

Masayuki Kimata (M)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.

Masasuke Ohno (M)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.

Noriyuki Suzaki (N)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.

Yasukazu Kajita (Y)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.

Tatsuo Takahashi (T)

Department of Neurosurgery, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.

Classifications MeSH