Repeated aortic dissection in a patient with autosomal dominant polycystic kidney disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,General Medicine,Surgery
Link
https://link.springer.com/content/pdf/10.1007/s11748-021-01756-5.pdf
Reference10 articles.
1. Ecder T. Cardiovascular complications in autosomal dominant polycystic kidney disease. Curr Hypertens Rev. 2013;9:2–11.
2. Silverio A, Prota C, Di Maio M, Polito MV, Cogliani FM, Citro R, et al. Aortic dissection in patients with autosomal dominant polycystic kidney disease: a series of two cases and a review of the literature. Nephrology (Carlton). 2015;20:229–35.
3. Evangelista A, Isselbacher EM, Bossone E, Gleason TG, Eusanio MD, Sechtem U, et al. Insights from the International Registry of Acute Aortic Dissection: a 20-year experience of collaborative clinical research. Circulation. 2018;137:1846–60.
4. Torres VE. Systemic manifestations of renal cystic disease. In: Gardner KD, Berstein J, editors. The cystic kidney. Dordrecht: Kluwer; 1990. p. 295–326.
5. Sung PH, Yang YH, Chiang HJ, Chiang JY, Chen CJ, Liu CT, et al. Risk of aortic aneurysm and dissection in patients with autosomal-dominant polycystic kidney disease: a nationwide population-based cohort study. Oncotarget. 2017;8:57594–604.
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