一名常染色体显性多囊肾病患者的胸主动脉夹层
Thoracic aortic dissection in a patient with autosomal dominant polycystic kidney disease.
作者信息
Adeola T, Adeleye O, Potts J L, Faulkner M, Oso A
机构信息
Department of Internal Medicine, Meharry Medical College, Nashville, Tennessee 37208, USA.
出版信息
J Natl Med Assoc. 2001 Jul-Aug;93(7-8):282-7.
Abstract
Autosomal dominant polycystic kidney disease is one of the most common hereditary diseases, and frequently has well defined extrarenal manifestations. Very few cases of aortic aneurysms associated with this disorder are described in literature. We report a 42-year-old male with autosomal dominant polycystic kidney disease presenting with dissecting aneurysm of the thoracic aorta.
摘要
常染色体显性多囊肾病是最常见的遗传性疾病之一，且常伴有明确的肾外表现。文献中很少描述与该疾病相关的主动脉瘤病例。我们报告了一名42岁患有常染色体显性多囊肾病的男性，其出现了胸主动脉夹层动脉瘤。
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