Division of Kidney and Pancreas Transplantation, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-Ro 43-Gil, Songpa-Gu, Seoul, 05505, Republic of Korea.
Department of Radiology and Research, Institute of Radiology, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Acta Neurochir (Wien). 2019 Nov;161(11):2389-2396. doi: 10.1007/s00701-019-04060-7. Epub 2019 Sep 9.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease, leading to kidney failure. One of the most serious extrarenal complications of ADPKD is comorbid intracranial aneurysms. The aim of this study is to evaluate the prevalence, rupture rate, and treatment outcomes of intracranial aneurysms in ADPKD.
Adult patients with a documented diagnosis of ADPKD who received kidney transplantation at our center from January 1994 to December 2018 were included in the study. Medical history, physical examination, laboratory findings, imaging studies, and operation records were collected and analyzed from our database.
Among 154 kidney transplant recipients with ADPKD, 113 (73.4%) patients were screened for intracranial aneurysms preoperatively. Twenty three patients (14.9%) had intracranial aneurysms with mean diameter size of 4.5 ± 2.7 mm. Nine patients (5.8%) experienced aneurysm rupture and the mean age at time of rupture was 34.9 ± 9.3 years. Twelve patients (52.2%) presented with multiple aneurysms. The most common aneurysm location was the bifurcation of the middle cerebral artery (34.9%). Clipping was the most common treatment in both ruptured and unruptured aneurysms.
Intracranial aneurysms are more frequent in patients with ADPKD, and the average age of intracranial artery rupture in patients with ADPKD is earlier than in the general population. It is necessary to consider proper evaluation and management of intracranial aneurysms when counseling ADPKD patients who will undergo kidney transplantation.
常染色体显性多囊肾病(ADPKD)是最常见的遗传性肾病,可导致肾衰竭。ADPKD 的最严重的肾外并发症之一是颅内伴发动脉瘤。本研究旨在评估 ADPKD 患者颅内动脉瘤的患病率、破裂率和治疗结果。
本研究纳入了 1994 年 1 月至 2018 年 12 月期间在我院接受肾移植的有明确 ADPKD 诊断的成年患者。从我们的数据库中收集并分析了患者的病史、体格检查、实验室检查结果、影像学研究和手术记录。
在 154 例 ADPKD 肾移植受者中,有 113 例(73.4%)患者在术前接受了颅内动脉瘤筛查。23 例(14.9%)患者存在颅内动脉瘤,平均直径为 4.5±2.7mm。9 例(5.8%)患者发生了动脉瘤破裂,破裂时的平均年龄为 34.9±9.3 岁。12 例(52.2%)患者存在多发性动脉瘤。最常见的动脉瘤部位是大脑中动脉分叉处(34.9%)。夹闭是破裂和未破裂动脉瘤最常用的治疗方法。
ADPKD 患者颅内动脉瘤更为常见,ADPKD 患者颅内动脉破裂的平均年龄早于普通人群。在为接受肾移植的 ADPKD 患者提供咨询时,有必要考虑对颅内动脉瘤进行适当的评估和管理。