Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease (ADPKD) is the most common congenital kidney disease. However, reports on occasional cases of aortic dissection in PKD familial patients remain scarce. Herein, we describe rare aortic dissection cases in PKD familial patients (i.e., mother and daughter) a...

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Autores principales: Inaba, Yu, Osako, Motohiko, Aoki, Michiko, Kasai, Mio, Yamabe, Kentaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese College of Angiology / The Japanese Society for Vascular Surgery / Japanese Society of Phlebology 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7991707/
https://www.ncbi.nlm.nih.gov/pubmed/33786104
http://dx.doi.org/10.3400/avd.cr.20-00149
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author Inaba, Yu
Osako, Motohiko
Aoki, Michiko
Kasai, Mio
Yamabe, Kentaro
author_facet Inaba, Yu
Osako, Motohiko
Aoki, Michiko
Kasai, Mio
Yamabe, Kentaro
author_sort Inaba, Yu
collection PubMed
description Autosomal dominant polycystic kidney disease (ADPKD) is the most common congenital kidney disease. However, reports on occasional cases of aortic dissection in PKD familial patients remain scarce. Herein, we describe rare aortic dissection cases in PKD familial patients (i.e., mother and daughter) and our successful treatment experience. The mother (84 years old) and daughter (53 years old) had a referral to us to treat type A acute aortic dissection. We performed emergency surgery and successfully treated the patients with an artificial graft. For comprehensive evaluation and treatment, ADPKD patients and their families should be screened for aortic diseases.
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spelling pubmed-79917072021-03-29 Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease Inaba, Yu Osako, Motohiko Aoki, Michiko Kasai, Mio Yamabe, Kentaro Ann Vasc Dis Case Report Autosomal dominant polycystic kidney disease (ADPKD) is the most common congenital kidney disease. However, reports on occasional cases of aortic dissection in PKD familial patients remain scarce. Herein, we describe rare aortic dissection cases in PKD familial patients (i.e., mother and daughter) and our successful treatment experience. The mother (84 years old) and daughter (53 years old) had a referral to us to treat type A acute aortic dissection. We performed emergency surgery and successfully treated the patients with an artificial graft. For comprehensive evaluation and treatment, ADPKD patients and their families should be screened for aortic diseases. Japanese College of Angiology / The Japanese Society for Vascular Surgery / Japanese Society of Phlebology 2021-03-25 /pmc/articles/PMC7991707/ /pubmed/33786104 http://dx.doi.org/10.3400/avd.cr.20-00149 Text en © 2021 The Editorial Committee of Annals of Vascular Diseases. http://creativecommons.org/licenses/by/2.5/ This article is distributed under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided the credit of the original work, a link to the license, and indication of any change are properly given, and the original work is not used for commercial purposes. Remixed or transformed contributions must be distributed under the same license as the original.
spellingShingle Case Report
Inaba, Yu
Osako, Motohiko
Aoki, Michiko
Kasai, Mio
Yamabe, Kentaro
Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
title Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
title_full Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
title_fullStr Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
title_full_unstemmed Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
title_short Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
title_sort aortic dissection in familial patients with autosomal dominant polycystic kidney disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7991707/
https://www.ncbi.nlm.nih.gov/pubmed/33786104
http://dx.doi.org/10.3400/avd.cr.20-00149
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