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自发性椎动脉夹层作为常染色体显性多囊肾病的一种并发症。

Spontaneous vertebral artery dissection as a complication of autosomal dominant polycystic kidney disease.

作者信息

Larranaga J, Rutecki G W, Whittier F C

机构信息

Department of Internal Medicine, Northeastern Ohio Universities College of Medicine, Affiliated Hospitals, Canton.

出版信息

Am J Kidney Dis. 1995 Jan;25(1):70-4. doi: 10.1016/0272-6386(95)90629-0.

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) may be associated with a variety of cardiovascular complications, including intracranial saccular aneurysms. In ADPKD, intracranial saccular aneurysms tend to rupture more frequently and earlier than the sporadic variety with a tendency to cluster in families. In contrast, dissecting intracranial aneurysms are rarely associated with either intracranial saccular aneurysms or ADPKD. We describe an ADPKD-1 patient whose course was complicated by a spontaneous dissection of a vertebral artery aneurysm. This particular patient had previously experienced three episodes of ascending aortic dissection with cystic medial necrosis. Intracranial vascular and aneurysmal dissection may occur in select ADPKD patients with familial clusters.

摘要

常染色体显性多囊肾病(ADPKD)可能与多种心血管并发症相关,包括颅内囊状动脉瘤。在ADPKD中,颅内囊状动脉瘤比散发性动脉瘤更易破裂且破裂时间更早,并且有家族聚集倾向。相比之下,夹层颅内动脉瘤很少与颅内囊状动脉瘤或ADPKD相关。我们描述了1例ADPKD - 1患者,其病程因椎动脉动脉瘤自发夹层而复杂化。该特殊患者先前曾经历3次升主动脉夹层伴囊性中层坏死。颅内血管和动脉瘤夹层可能发生在有家族聚集性的特定ADPKD患者中。

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