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Prevalence of Intracranial Aneurysms in Patients with Connective Tissue Diseases: A Retrospective Study.结缔组织病患者颅内动脉瘤的患病率:一项回顾性研究。
AJNR Am J Neuroradiol. 2016 Aug;37(8):1422-6. doi: 10.3174/ajnr.A4718. Epub 2016 Mar 18.
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Controversies in epidemiology of intracranial aneurysms and SAH.颅内动脉瘤和蛛网膜下腔出血的流行病学争议。
Nat Rev Neurol. 2016 Jan;12(1):50-5. doi: 10.1038/nrneurol.2015.228. Epub 2015 Dec 16.
3
Increased Risk of Cerebrovascular Disease Among Patients With Neurofibromatosis Type 1: Population-Based Approach.1型神经纤维瘤病患者脑血管疾病风险增加:基于人群的研究方法
Stroke. 2016 Jan;47(1):60-5. doi: 10.1161/STROKEAHA.115.011406. Epub 2015 Dec 8.
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High prevalence of elevated blood pressure among children with neurofibromatosis type 1.1型神经纤维瘤病患儿中高血压患病率高。
Pediatr Nephrol. 2016 Jan;31(1):131-6. doi: 10.1007/s00467-015-3191-6. Epub 2015 Aug 28.
5
Giant malignant peripheral nerve sheath tumor with cauda equina syndrome and subarachnoid hemorrhage: Complications in a case of type 1 neurofibromatosis.伴有马尾综合征和蛛网膜下腔出血的巨大恶性外周神经鞘瘤:1型神经纤维瘤病1例的并发症
J Nat Sci Biol Med. 2015 Jul-Dec;6(2):436-9. doi: 10.4103/0976-9668.160029.
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Epilepsy after aneurysmal subarachnoid hemorrhage: A population-based, long-term follow-up study.动脉瘤性蛛网膜下腔出血后的癫痫:一项基于人群的长期随访研究。
Neurology. 2015 Jun 2;84(22):2229-37. doi: 10.1212/WNL.0000000000001643. Epub 2015 May 6.
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Incidence and mortality of neurofibromatosis: a total population study in Finland.神经纤维瘤病的发病率和死亡率:芬兰的一项全人群研究。
J Invest Dermatol. 2015 Mar;135(3):904-906. doi: 10.1038/jid.2014.465. Epub 2014 Oct 29.
8
Neurofibromatosis type 1: a multidisciplinary approach to care.神经纤维瘤病 1 型:多学科护理方法。
Lancet Neurol. 2014 Aug;13(8):834-43. doi: 10.1016/S1474-4422(14)70063-8.
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Unruptured intracranial aneurysms: epidemiology, natural history, management options, and familial screening.未破裂颅内动脉瘤:流行病学、自然史、治疗选择和家族筛查。
Lancet Neurol. 2014 Apr;13(4):393-404. doi: 10.1016/S1474-4422(14)70015-8.
10
Circle of Willis abnormalities in children with neurofibromatosis type 1.儿童 1 型神经纤维瘤病患者的 Willis 环异常。
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1型神经纤维瘤病与蛛网膜下腔出血无关。

Neurofibromatosis type 1 is not associated with subarachnoid haemorrhage.

作者信息

Kurtelius Arttu, Kallionpää Roope A, Huttunen Jukka, Huttunen Terhi J, Helin Katariina, Koivisto Timo, Frösen Juhana, von Und Zu Fraunberg Mikael, Peltonen Sirkku, Peltonen Juha, Jääskeläinen Juha E, Lindgren Antti E

机构信息

Neurosurgery, NeuroCenter, Kuopio University Hospital, Kuopio, Finland.

Neurosurgery, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.

出版信息

PLoS One. 2017 Jun 2;12(6):e0178711. doi: 10.1371/journal.pone.0178711. eCollection 2017.

DOI:10.1371/journal.pone.0178711
PMID:28575128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5456355/
Abstract

BACKGROUND

The prevalence of intracranial aneurysms (IAs) has been proposed to be elevated in the patients with neurofibromatosis type 1 (NF1). Our aims were to determine the prevalence of NF1 in a large Finnish population based cohort of IA patients and, on the other hand, the occurrences of subarachnoid haemorrhage and unruptured intracranial aneurysms in a nationwide population-based cohort of NF1 patients and its matched ten-fold control cohort.

METHODS

The Kuopio IA Database (www.kuopioneurosurgery.fi) includes all ruptured and unruptured IA cases admitted to the Kuopio University Hospital (KUH) from its defined Eastern Finnish catchment population since 1980. In this registry-based study, we cross-linked the Kuopio IA database with the Finnish national registry covering all hospital diagnoses. The NF1 diagnoses of the 4543 patients with either saccular of fusiform IA were identified from 1969 to 2015 and verified from patient records. Our second approach was to analyze the occurrence of aneurysmal subarachnoid haemorrhage (aSAH) and unruptured IAs in a nationwide population-based database of 1410 NF1 patients and its ten-fold matched control cohort (n = 14030) using national registry of hospital diagnoses between 1987 and 2014.

RESULTS

One NF1 patient was identified among the 4543 IA patients. Three verified IA cases (one unruptured IA and two aSAH cases) were identified in the cohort of 1410 NF1 patients, with similar occurrences in the control cohort.

CONCLUSIONS

We found no evidence in our population-based cohorts to support the conception that NF1 is associated with IAs. Our results indicate that the incidence of aSAH is not elevated in patients with NF1. Further studies are required to confirm that there is no association between NF1 and unruptured IAs.

摘要

背景

有研究提出,1型神经纤维瘤病(NF1)患者颅内动脉瘤(IA)的患病率有所升高。我们的目的是确定在芬兰一个大型基于人群队列的IA患者中NF1的患病率,另一方面,确定在全国范围内基于人群队列的NF1患者及其匹配的十倍规模对照队列中蛛网膜下腔出血和未破裂颅内动脉瘤的发生率。

方法

库奥皮奥IA数据库(www.kuopioneurosurgery.fi)包含自1980年以来从芬兰东部特定集水区人群收治到库奥皮奥大学医院(KUH)的所有破裂和未破裂IA病例。在这项基于登记处的研究中,我们将库奥皮奥IA数据库与涵盖所有医院诊断的芬兰国家登记处进行了交叉链接。从1969年至2015年确定了4543例囊状或梭形IA患者的NF1诊断,并从患者记录中进行了核实。我们的第二种方法是使用1987年至2014年的医院诊断国家登记处,分析在一个包含1410例NF1患者的全国性基于人群的数据库及其十倍规模匹配对照队列(n = 14030)中动脉瘤性蛛网膜下腔出血(aSAH)和未破裂IA的发生率。

结果

在4543例IA患者中识别出1例NF1患者。在1410例NF1患者队列中识别出3例经核实的IA病例(1例未破裂IA和2例aSAH病例),在对照队列中的发生率相似。

结论

在我们基于人群的队列中,没有证据支持NF1与IA相关的观点。我们的结果表明,NF1患者中aSAH的发生率没有升高。需要进一步研究以证实NF1与未破裂IA之间不存在关联。