| Literature DB >> 33786104 |
Yu Inaba1, Motohiko Osako1, Michiko Aoki1, Mio Kasai1, Kentaro Yamabe1.
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.Entities:
Keywords: ADPKD; aortic dissection
Year: 2021 PMID: 33786104 PMCID: PMC7991707 DOI: 10.3400/avd.cr.20-00149
Source DB: PubMed Journal: Ann Vasc Dis ISSN: 1881-641X