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DOI 10.5761/atcs.cr.11.01756

Медицинская библиотека · Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia · 2012

Dissecting aneurysm in a patient with autosomal dominant polycystic kidney disease.

Fukunaga Naoto, Yuzaki Mitsuru, Nasu Michihiro, Okada Yukikatsu

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Аннотация

Autosomal dominant polycystic kidney disease (ADPKD) is primarily associated with renal failure, but it also causes systemic diseases, including cysts of other systemic organs and cerebral or visceral aneurysm. To make matters worse, life-threatening aortic diseases are associated with ADPKD in some cases. However, only a few reports of ADPKD-associated with thoracic aortic dissection have been published. Herein, we present a case of dissecting aneurysm in a patient with hypertension and ADPKD. He had been followed up for type B aortic dissection for six years. Preoperative creatinine level ranged from 2.1 to 2.4 mg/dl. We performed replacement of the thoracic aorta with prosthetic graft successfully, and postoperatively, dialysis was not required.It is very important for us to recognize the relationship between ADPKD and thoracic aortic dissection, which can cause high mortality and morbidity rates.

Для цитирования: Fukunaga Naoto, Yuzaki Mitsuru, Nasu Michihiro, Okada Yukikatsu. Dissecting aneurysm in a patient with autosomal dominant polycystic kidney disease.. Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia. 2012. DOI: 10.5761/atcs.cr.11.01756.

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