Unruptured intracranial aneurysms in pediatric sickle cell disease: clinical and MR imaging follow-up of 296 patients.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY Journal of neurosurgery. Pediatrics Pub Date : 2024-09-27 DOI:10.3171/2024.7.PEDS24231
Deepak Khatri, Richard Zampolin, Adisson Fortunel, Seon-Kyu Lee
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Abstract

Objective: Currently available data regarding unruptured intracranial aneurysms (UIAs) in sickle cell disease (SCD) are largely based on adult patients; this has made it challenging to reach a consensus on treatment decisions and follow-up strategies for pediatric SCD patients with UIAs.

Methods: A retrospective review of 296 SCD patients (aged 18 years or younger) who underwent MRA from January 2008 to September 2022 was performed. The vessel of origin and characteristics of the UIAs, including maximum diameter, laterality, and number, were evaluated. Demographic data, as well as history of vaso-occlusive crisis and moyamoya syndrome, were recorded. Interval change in size or morphology, as well as a new aneurysm development, were reviewed on follow-up MRA.

Results: Forty-nine aneurysms were identified in 32/296 (10.81%) patients, and they all had saccular morphology. In total, 30/49 (61.22%) aneurysms were in the anterior circulation. The ophthalmic segment of the internal carotid artery and the posterior cerebral artery were the most common locations (n = 12 [24.49%] each). Multiple aneurysms were seen in 11/32 patients (34.37%). Most of the African American patients had multiple aneurysms (n = 25/28 [89.3%]). Most aneurysms (n = 43 [87.75%]) were 3 mm or less in diameter. No significant difference in aneurysm size was noticed between aneurysms located in anterior or posterior circulation (p = 0.22). Similarly, age, sex, ethnicity, genotype, or aneurysm multiplicity were not associated with size. Follow-up MRA was available for 24/32 patients (75%). All except 2 aneurysms (n = 2/38 [5.3%]) were stable in size and morphology on follow-up. Interval progression in aneurysm size was noticed in 2 patients with multiple intracranial aneurysms (n = 2/11 [18.2%]).

Conclusions: In pediatric SCD patients, the incidence of UIAs was higher than previously reported. Those aneurysms demonstrated a tendency for multiplicity, an atypical anatomical distribution compared with that of adult brain aneurysms, bilateral involvement, and higher prevalence in African Americans. Although most of the aneurysms were stable, some showed interval growth in size.

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小儿镰状细胞病未破裂的颅内动脉瘤:296 例患者的临床和磁共振成像随访。
目的:目前有关镰状细胞病(SCD)未破裂颅内动脉瘤(UIAs)的现有数据主要基于成人患者;这使得就患有 UIAs 的儿童 SCD 患者的治疗决策和随访策略达成共识具有挑战性:方法: 对 2008 年 1 月至 2022 年 9 月期间接受 MRA 检查的 296 例 SCD 患者(18 岁或以下)进行了回顾性研究。评估了 UIA 的起源血管和特征,包括最大直径、侧位和数量。此外,还记录了人口统计学数据以及血管闭塞危象和莫亚莫亚综合征病史。在随访的 MRA 中审查了大小或形态的间隔变化,以及新动脉瘤的发展情况:结果:32/296(10.81%)例患者中发现了 49 个动脉瘤,均为囊状形态。其中,30/49(61.22%)个动脉瘤位于前循环。颈内动脉眼段和大脑后动脉是最常见的位置(各为 12 个 [24.49%])。多发性动脉瘤见于 11/32 例患者(34.37%)。大多数非裔美国人患者有多个动脉瘤(n = 25/28 [89.3%])。大多数动脉瘤(n = 43 [87.75%])的直径为 3 毫米或更小。位于前循环或后循环的动脉瘤大小无明显差异(P = 0.22)。同样,年龄、性别、种族、基因型或动脉瘤多发性也与动脉瘤大小无关。有 24/32 例患者(75%)获得了随访 MRA。除 2 个动脉瘤(n = 2/38 [5.3%])外,其他所有动脉瘤的大小和形态在随访期间均保持稳定。在 2 例多发性颅内动脉瘤患者(n = 2/11 [18.2%])中,动脉瘤的大小出现了间隔性进展:结论:在小儿 SCD 患者中,UIA 的发病率高于之前的报道。结论:在小儿 SCD 患者中,UIAs 的发病率高于之前的报道。这些动脉瘤有多发性趋势,与成人脑动脉瘤相比,解剖分布不典型,双侧受累,非裔美国人发病率更高。虽然大多数动脉瘤都比较稳定,但有些动脉瘤的大小呈间歇性增长。
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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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