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- Title
Intracranial aneurysms in patients receiving kidney transplantation for autosomal dominant polycystic kidney disease.
- Authors
Kim, Jee Yeon; Jung, Seung Chai; Ko, Youngmin; Kim, Dong Hyun; Choi, Ji Yoon; Kwon, Hyunwook; Jung, Joo Hee; Kim, Young Hoon; Han, Duck Jong; Shin, Sung
- Abstract
Background: 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. Methods: 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. Results: 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. Conclusions: 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.
- Subjects
POLYCYSTIC kidney disease; INTRACRANIAL aneurysms; KIDNEY transplantation; GENETIC disorders
- Publication
Acta Neurochirurgica, 2019, Vol 161, Issue 11, p2389
- ISSN
0001-6268
- Publication type
Article
- DOI
10.1007/s00701-019-04060-7