| Literature DB >> 31092765 |
Kazuki Ueda1, Eriko Morishita2, Hironaga Shiraki3, Shunzo Matsuoka3, Shinsaku Imashuku4.
Abstract
Thrombophilia increases the risk of venous thrombosis, but is rarely responsible for aortic thrombosis. Aortic mural thrombus (AMT) may be associated with a protein C deficiency. However, it is necessary to determine whether the protein C deficiency is congenital/hereditary or secondary/acquired (consumption of protein C during the process of thrombus formation). This study describes a 77-year-old Japanese woman with incidentally diagnosed AMT, who had a protein C deficiency (activity 54%, antigen 42%). Sequencing of the protein C gene revealed a heterozygous mutation of c.1268delG, p.Gly423Valfs*82 in exon 9, indicating a congenital protein C deficiency. These findings indicate that very late onset AMT can occur in an adult with congenital protein C deficiency.Entities:
Keywords: Aortic mural thrombosis; Congenital thrombophilia; Protein C deficiency
Year: 2019 PMID: 31092765 PMCID: PMC6976720 DOI: 10.5551/jat.48819
Source DB: PubMed Journal: J Atheroscler Thromb ISSN: 1340-3478 Impact factor: 4.928