表现为蛛网膜下腔出血的常染色体显性遗传性多囊肾病

Autosomal dominant polycystic kidney disease presenting as subarachnoid hemorrhage.

作者信息

Kanne Jeffrey P, Talner Lee B

机构信息

Department of Radiology, Harborview Medical Center, University of Washington School of Medicine, 325 Ninth Ave, Box 359728, Seattle, WA 98104-2499, USA.

出版信息

Emerg Radiol. 2004 Dec;11(2):110-2. doi: 10.1007/s10140-004-0357-0.

DOI:10.1007/s10140-004-0357-0

PMID:15801061

Abstract

Intracranial aneurysms occur in patients with autosomal dominant polycystic kidney disease (ADPKD) approximately five times more often than in the general population, and in the same patient group, subarachnoid hemorrhage from rupture of aneurysms occurs about a decade earlier than in the general population. We present a case of unsuspected ADPKD presenting as spontaneous subarachnoid hemorrhage from a ruptured intracranial aneurysm.

摘要

颅内动脉瘤在常染色体显性遗传性多囊肾病（ADPKD）患者中的发生率比普通人群高约五倍，并且在同一患者群体中，动脉瘤破裂导致的蛛网膜下腔出血比普通人群早大约十年。我们报告一例未被怀疑患有ADPKD的患者，其因颅内动脉瘤破裂而出现自发性蛛网膜下腔出血。