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Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient

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 (co...

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Autores principales: Ueda, Kazuki, Morishita, Eriko, Shiraki, Hironaga, Matsuoka, Shunzo, Imashuku, Shinsaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976720/
https://www.ncbi.nlm.nih.gov/pubmed/31092765
http://dx.doi.org/10.5551/jat.48819
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author Ueda, Kazuki
Morishita, Eriko
Shiraki, Hironaga
Matsuoka, Shunzo
Imashuku, Shinsaku
author_facet Ueda, Kazuki
Morishita, Eriko
Shiraki, Hironaga
Matsuoka, Shunzo
Imashuku, Shinsaku
author_sort Ueda, Kazuki
collection PubMed
description 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.
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spelling pubmed-69767202020-01-29 Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient Ueda, Kazuki Morishita, Eriko Shiraki, Hironaga Matsuoka, Shunzo Imashuku, Shinsaku J Atheroscler Thromb Case Report 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. Japan Atherosclerosis Society 2020-01-01 /pmc/articles/PMC6976720/ /pubmed/31092765 http://dx.doi.org/10.5551/jat.48819 Text en 2020 Japan Atherosclerosis Society This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Case Report
Ueda, Kazuki
Morishita, Eriko
Shiraki, Hironaga
Matsuoka, Shunzo
Imashuku, Shinsaku
Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
title Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
title_full Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
title_fullStr Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
title_full_unstemmed Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
title_short Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
title_sort aortic mural thrombus associated with congenital protein c deficiency in an elderly patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976720/
https://www.ncbi.nlm.nih.gov/pubmed/31092765
http://dx.doi.org/10.5551/jat.48819
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