scholarly journals Acute Aortic Dissection Associated with Adult Autosomal Dominant Polycystic Kidney Disease: Three Case Reports and a Review

2007 ◽  
Vol 3 (1) ◽  
pp. 25-29
Author(s):  
Yuki Nakamura ◽  
Hiroko Yotsukura ◽  
Masahiko Kato ◽  
Jun Nakat ◽  
Keiji Tanaka ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Aortic Dissection ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Acute Aortic Dissection ◽  
Case Reports ◽  
Polycystic Kidney ◽  
Autosomal Dominant Polycystic Kidney

Autosomal dominant polycystic kidney disease associated with aortic dissection: Two case reports

1997 ◽  
Vol 1 (4) ◽  
pp. 288-291 ◽  
Author(s):  
Takashi Fujii ◽  
Takashi Uzu ◽  
Satoko Nakamura ◽  
Takashi Inenaga ◽  
Motomi Ando ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Aortic Dissection ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Case Reports ◽  
Polycystic Kidney ◽  
Autosomal Dominant Polycystic Kidney

The coexistence of acute aortic dissection with autosomal dominant polycystic kidney disease - description of two hypertensive patients

2004 ◽  
Vol 13 (5) ◽  
pp. 283-286 ◽  
Author(s):  
Mariola Pe¸czkowska ◽  
Andrzej Januszewicz ◽  
Władysław Grzeszczak ◽  
Dariusz Moczulski ◽  
Hanna Janaszek-sitkowska ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Aortic Dissection ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Acute Aortic Dissection ◽  
Polycystic Kidney ◽  
Hypertensive Patients ◽  
Autosomal Dominant Polycystic Kidney

scholarly journals Aortic dissection in patients with autosomal dominant polycystic kidney disease: A series of two cases and a review of the Literature

Nephrology ◽  
2015 ◽  
Vol 20 (4) ◽  
pp. 229-235 ◽  
Author(s):  
Angelo Silverio ◽  
Costantina Prota ◽  
Marco Di Maio ◽  
Maria Vincenza Polito ◽  
Francesco Maria Cogliani ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Aortic Dissection ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
Review Of The Literature ◽  
Polycystic Kidney ◽  
Autosomal Dominant Polycystic Kidney

scholarly journals Aortic Dissection Associated with Autosomal Dominant Polycystic Kidney Disease: A Case Report

2019 ◽  
Vol 22 (1) ◽  
pp. E032-E034 ◽  
Author(s):  
Shigeaki Aoyagi ◽  
Takeshi Oda ◽  
Ryo Kanamoto ◽  
Eiji Nakamura ◽  
Hiroshi Yasunaga
Keyword(s):  
Kidney Disease ◽  
Aortic Dissection ◽  
Polycystic Kidney Disease ◽  
Autosomal Dominant ◽  
False Lumen ◽  
Ascending Aorta ◽  
Polycystic Kidney ◽  
Thrombotic Occlusion ◽  
Autosomal Dominant Polycystic Kidney ◽  
Intimal Tear

A 78-year-old man who had been diagnosed with autosomal dominant polycystic kidney disease (ADPKD) and hypertension presented with chest pain. His family history was positive for ADPKD. Chest computed tomography (CT) revealed a type A aortic dissection with thrombotic occlusion of a false lumen and an ulcer-like projection in the ascending aorta, an aneurysm of the ascending aorta, and pericardial effusion. Abdominal CT showed multiple renal and hepatic cysts. At surgery, aortic dissection with thrombotic occlusion of the false lumen and an intimal tear in the distal ascending aorta were observed. Hemiarch replacement including the intimal tear was performed. The patient is doing well without requiring dialysis and without recurrence of aortic dissection or aneurysm under strict antihypertensive therapy 3 years after the operation. Pathological examination of aortic wall specimens revealed no degenerative abnormality. ADPKD should be kept in mind as one of the causative disorders of aortic dissection.

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