Ontology highlight
ABSTRACT:
SUBMITTER: Kamio S
PROVIDER: S-EPMC8495039 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature
Kamio Satoru S Kubo Takatoshi T Koshino Saori S Abe Osamu O
Radiology case reports 20211001 12
ACTA2-related vasculopathy is an autosomal dominant genetic disorder characterized by aortic aneurysms and dissection, and limb artery lesions are rare. We report a case of transcatheter arterial embolization for a pseudoaneurysm of a deep femoral artery in a patient with presumptive ACTA2-related vasculopathy. A 58-year-old woman was presumed to have an <i>ACTA2</i> mutation based on her history of aortic diseases and family history of <i>ACTA2</i> mutations. During follow-up, contrast-enhanced ...[more]