Related Experiment Video
Updated: Nov 11, 2025

Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium
Published on: September 1, 2015
Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease
Yu Inaba1, Motohiko Osako1, Michiko Aoki1
1Department of Cardiovascular Surgery, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Abstract:
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.
Related Concept Videos
Aortic Regurgitation II: Clinical Features and Diagnostic Tests
Nephrons
Chronic Kidney Disease I: Introduction
Aneurysm I: Introduction
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Pedigree Analysis

