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儿童未破裂颅内动脉瘤:三级护理儿科机构18年的经验

Unruptured intracranial aneurysms in children: 18 years' experience in a tertiary care pediatric institution.

作者信息

Bisson Daniel-Alexandre, Dirks Peter, Amirabadi Afsaneh, Shroff Manohar M, Krings Timo, Pereira Vitor Mendes, Muthusami Prakash

机构信息

1Department of Diagnostic Imaging, The Hospital for Sick Children, University of Toronto, Ontario.

2Division of Neurosurgery, Department of Surgery, University of Toronto, Ontario; and.

出版信息

J Neurosurg Pediatr. 2019 May 24;24(2):184-189. doi: 10.3171/2019.4.PEDS18703. Print 2019 Aug 1.

Abstract

OBJECTIVE

There are little data in the literature on the characteristics and natural history of unruptured intracranial aneurysms in children. The authors analyzed their experience with unruptured intracranial aneurysms in the pediatric population at their tertiary care pediatric institution over the last 18 years. The first objective was to assess the imaging characteristics and natural history of these aneurysms in order to help guide management strategies in the future. A second objective was to evaluate the frequency of an underlying condition when an incidental intracranial aneurysm was detected in a child.

METHODS

The authors conducted a Research Ethics Board-approved retrospective review of incidental intracranial aneurysms in patients younger than 18 years of age who had been treated at their institution in the period from 1998 to 2016. Clinical (age, sex, syndrome) and radiological (aneurysm location, type, size, thrombus, mass effect) data were recorded. Follow-up imaging was assessed for temporal changes.

RESULTS

Sixty intracranial aneurysms occurred in 51 patients (36 males, 15 females) with a mean age of 10.5 ± 0.5 years (range 9 months-17 years). Forty-five patients (88.2%) had a single aneurysm, while 2 and 3 aneurysms were found in 3 patients each (5.8%). Syndromic association was found in 22 patients (43.1%), most frequently sickle cell disease (10/22 [45.5%]). Aneurysms were saccular in 43 cases (71.7%; mean size 5.0 ± 5.7 mm) and fusiform in the remaining 17 (28.3%; mean size 6.5 ± 2.7 mm). Thirty-one aneurysms (51.7%) arose from the internal carotid artery (right/left 1.4), most commonly in the cavernous segment (10/31 [32.3%]). Mean size change over the entire follow-up of 109 patient-years was a decrease of 0.6 ± 4.2 mm (range -30.0 to +4.0 mm, rate -0.12 ± 9.9 mm/yr). Interval growth (2.0 ± 1.0 mm) was seen in 8 aneurysms (13.3%; 4 saccular, 4 fusiform). An interval decrease in size (8.3 ± 10.7 mm) was seen in 6 aneurysms (10%). There was an inverse relationship between aneurysm size and growth rate (r = -0.82, p < 0.00001). One aneurysm was treated endovascularly with internal carotid artery sacrifice.

CONCLUSIONS

Unruptured pediatric intracranial aneurysms are most frequently single but can occur in multiples in a syndromic setting. None of the cases from the study period showed clinical or imaging signs of rupture. Growth over time, although unusual and slow, can occur in a proportion of these patients, who should be identified for short-term imaging surveillance.

摘要

目的

文献中关于儿童未破裂颅内动脉瘤的特征和自然史的数据很少。作者分析了他们在过去18年中在三级医疗儿科机构对儿科人群未破裂颅内动脉瘤的治疗经验。第一个目标是评估这些动脉瘤的影像学特征和自然史,以帮助指导未来的管理策略。第二个目标是评估在儿童中检测到偶然颅内动脉瘤时潜在疾病的发生率。

方法

作者对1998年至2016年期间在其机构接受治疗的18岁以下患者的偶然颅内动脉瘤进行了一项经研究伦理委员会批准的回顾性研究。记录临床(年龄、性别、综合征)和放射学(动脉瘤位置、类型、大小、血栓、占位效应)数据。评估随访影像学检查的时间变化。

结果

51例患者(36例男性,15例女性)发生了60个颅内动脉瘤,平均年龄为10.5±0.5岁(范围9个月至17岁)。45例患者(88.2%)有单个动脉瘤,3例患者各发现2个和3个动脉瘤(5.8%)。22例患者(43.1%)存在综合征关联,最常见的是镰状细胞病(10/22 [45.5%])。43例动脉瘤为囊状(71.7%;平均大小5.0±5.7mm),其余17例为梭形(28.3%;平均大小6.5±2.7mm)。31个动脉瘤(51.7%)起源于颈内动脉(右侧/左侧1.4),最常见于海绵窦段(10/31 [32.3%])。在109患者年的整个随访期间,平均大小变化为减少0.6±4.2mm(范围-30.0至+4.0mm,速率-0.12±9.9mm/年)。8个动脉瘤(13.3%;4个囊状,4个梭形)出现间隔性生长(2.0±1.0mm)。6个动脉瘤(10%)出现大小间隔性减小(8.3±10.7mm)。动脉瘤大小与生长速率之间存在负相关(r = -0.82,p < 0.00001)。1个动脉瘤通过颈内动脉牺牲进行了血管内治疗。

结论

未破裂的儿童颅内动脉瘤最常见为单个,但在综合征情况下可多发。研究期间的所有病例均未显示破裂的临床或影像学征象。随着时间的推移,尽管这些患者中一部分的生长不常见且缓慢,但仍可能发生,应确定这些患者进行短期影像学监测。

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