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- W4378953114 abstract "Whereas cerebral aneurysm is a well-known consequence of autosomal dominant polycystic kidney disease (ADPKD), acute aortic dissection has been rarely reported. A patient was a 44-year-old male with a diagnosis of ADPKD, who had previously undergone transcatheter arterial embolization for a renal cyst hemorrhage. He presented with sudden onset of back pain, which got worse at emergency service. Contrast-enhanced computed tomography (CT) revealed Stanford type A acute aortic dissection. The patient subsequently underwent partial aortic arch replacement with a vascular graft under circulatory arrest. His postoperative course was complicated by pneumonia and required ventilation support for a week. Peak creatinine level was 3.28 mg/dl, but hemodialysis was not required. Patients with ADPKD should be considered a high-risk cohort of aortic dissection." @default.
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- W4378953114 date "2023-06-01" @default.
- W4378953114 modified "2023-09-24" @default.
- W4378953114 title "[Stanford Type A Acute Aortic Dissection Associated with Polycystic Kidney Disease]." @default.
- W4378953114 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37258017" @default.
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