Case Report: Spontaneous Postpartum Quadruple Cervicocephalic Arterial Dissection With a Heterozygous
COL5A1 gene mutation
cervicocephalic arterial dissection
postpartum
pregnancy
quadruple
Journal
Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899
Informations de publication
Date de publication:
2022
2022
Historique:
received:
26
04
2022
accepted:
20
06
2022
entrez:
1
8
2022
pubmed:
2
8
2022
medline:
2
8
2022
Statut:
epublish
Résumé
Pregnancy-associated cervicocephalic arterial dissection is rare, and its pathophysiology remains poorly understood. Despite the hypothesized contribution to pathogenesis, connective tissue diseases and genetic factors are rarely identified in clinical cases. We describe a case of postpartum arterial dissection involving all four cervicocephalic arteries resulting in acute cerebral infarction. The patient underwent successful endovascular thrombectomy and angioplasty and recovered fully without sequelae. Genetic screening for connective tissue diseases identified a heterozygous missense
Identifiants
pubmed: 35911880
doi: 10.3389/fneur.2022.928803
pmc: PMC9327320
doi:
Types de publication
Case Reports
Langues
eng
Pagination
928803Informations de copyright
Copyright © 2022 Imamura, Omura, Sasaki, Arino, Nohara, Saito, Ichinose, Yamaguchi, Kojima, Inagawa, Takahashi, Unno, Morisaki, Ishikawa, Yoshikawa and Okada.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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