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An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal and extrarenal, cystic and noncystic manifestations. Connective tissue defects, including cerebral aneurysm, meningeal diverticula, abdominal wall hernias, intestinal diverticula, and cardiac valvular...

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Autores principales: Catapano, Fausta, Pancaldi, Stefano, Napoleone, Carlo Pace, De Sanctis, Lucia Barbara, Gargiulo, Gaetano, Emiliani, Giuseppe, Santoro, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914240/
https://www.ncbi.nlm.nih.gov/pubmed/24558619
http://dx.doi.org/10.1155/2012/978170
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author Catapano, Fausta
Pancaldi, Stefano
Napoleone, Carlo Pace
De Sanctis, Lucia Barbara
Gargiulo, Gaetano
Emiliani, Giuseppe
Santoro, Antonio
author_facet Catapano, Fausta
Pancaldi, Stefano
Napoleone, Carlo Pace
De Sanctis, Lucia Barbara
Gargiulo, Gaetano
Emiliani, Giuseppe
Santoro, Antonio
author_sort Catapano, Fausta
collection PubMed
description Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal and extrarenal, cystic and noncystic manifestations. Connective tissue defects, including cerebral aneurysm, meningeal diverticula, abdominal wall hernias, intestinal diverticula, and cardiac valvular abnormalities, are widely known manifestations. Instead intracardiac aneurysms have never been reported in adults with autosomal dominant polycystic kidney disease. We describe a 65-year-old patient with end-stage renal disease due to autosomal dominant polycystic kidney disease and an atrial septum aneurysm associated with platypnoea-orthodeoxia syndrome.
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spelling pubmed-39142402014-02-20 An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease Catapano, Fausta Pancaldi, Stefano Napoleone, Carlo Pace De Sanctis, Lucia Barbara Gargiulo, Gaetano Emiliani, Giuseppe Santoro, Antonio Case Rep Nephrol Case Report Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal and extrarenal, cystic and noncystic manifestations. Connective tissue defects, including cerebral aneurysm, meningeal diverticula, abdominal wall hernias, intestinal diverticula, and cardiac valvular abnormalities, are widely known manifestations. Instead intracardiac aneurysms have never been reported in adults with autosomal dominant polycystic kidney disease. We describe a 65-year-old patient with end-stage renal disease due to autosomal dominant polycystic kidney disease and an atrial septum aneurysm associated with platypnoea-orthodeoxia syndrome. Hindawi Publishing Corporation 2012 2012-11-22 /pmc/articles/PMC3914240/ /pubmed/24558619 http://dx.doi.org/10.1155/2012/978170 Text en Copyright © 2012 Fausta Catapano et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Catapano, Fausta
Pancaldi, Stefano
Napoleone, Carlo Pace
De Sanctis, Lucia Barbara
Gargiulo, Gaetano
Emiliani, Giuseppe
Santoro, Antonio
An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
title An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
title_full An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
title_fullStr An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
title_full_unstemmed An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
title_short An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
title_sort unusual cardiac manifestation in autosomal dominant polycystic kidney disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914240/
https://www.ncbi.nlm.nih.gov/pubmed/24558619
http://dx.doi.org/10.1155/2012/978170
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