A Case of Severe Aortic Valve Regurgitation Caused by an Ascending Aortic Aneurysm in a Young Patient With Autosomal Dominant Polycystic Kidney Disease and Normal Renal Function.
10.4070/kcj.2012.42.2.136
- Author:
Jeongeun KIM
1
;
Sang Min KIM
;
Sang Yeub LEE
;
Ho Chang LEE
;
Jang Whan BAE
;
Kyung Kuk HWANG
;
Dong Woon KIM
;
Myeong Chan CHO
;
Sun Ju BYEON
;
Ki Bong KIM
Author Information
1. Regional Cardiovascular Center, Division of Cardiology, Department of Internal Medicine, Chungbuk National University School of Medicine, Cheongju, Korea. drcorazon@hanmail.net
- Publication Type:Case Report
- Keywords:
Aortic regurgitation;
Aortic aneurysm, thoracic;
Polycystic kidney, autosomal dominant
- MeSH:
Adult;
Aneurysm;
Aorta, Abdominal;
Aorta, Thoracic;
Aortic Aneurysm;
Aortic Aneurysm, Thoracic;
Aortic Valve;
Aortic Valve Insufficiency;
Asian Continental Ancestry Group;
Humans;
Hypertension;
Male;
Polycystic Kidney, Autosomal Dominant;
Stress, Psychological
- From:Korean Circulation Journal
2012;42(2):136-139
- CountryRepublic of Korea
- Language:English
-
Abstract:
Aortic aneurysm is one several well-known cardiovascular complications in patients with autosomal dominant polycystic kidney disease (ADPCKD). Commonly affected site of aortic aneurysm and its related dissection in ADPCKD is abdominal aorta. Long standing hypertension, haemodialysis, old age are closely related with discovering of aortic aneurysm and dissection in ADPCKD. However, thoracic aortic aneurysms and its related severe aortic regurgitations (ARs) are rare in younger patients suffering from ADPCKD, especially ones who have normal renal function. Here, we report a case involving a 27-year-old Asian male patient with severe AR due to an ascending aneurysm of the thoracic aorta associated with ADPCKD. The patient had normal renal function without Marfan's habitus. The AR and thoracic aortic aneurysm were corrected surgically.
