Suppr超能文献

小儿镰状细胞病未破裂颅内动脉瘤:296 例患者的临床和磁共振成像随访。

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

机构信息

Departments of1Radiology.

3Neurosurgery, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.

出版信息

J Neurosurg Pediatr. 2024 Sep 27;34(6):585-590. doi: 10.3171/2024.7.PEDS24231. Print 2024 Dec 1.

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.

摘要

目的

目前关于镰状细胞病(SCD)中未破裂颅内动脉瘤(UIAs)的数据主要基于成年患者;这使得在治疗决策和患有 UIAs 的儿科 SCD 患者的随访策略方面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 的 296 例 SCD 患者(年龄在 18 岁以下)进行回顾性分析。评估了动脉瘤的起源血管和特征,包括最大直径、偏侧性和数量。记录了人口统计学数据,以及血管阻塞性危机和烟雾病的病史。在随访 MRA 上回顾了大小或形态的间隔变化以及新动脉瘤的发展。

结果

在 32/296(10.81%)名患者中发现了 49 个动脉瘤,它们均呈囊状形态。总共 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部位(各有 12 个[24.49%])。11/32 名患者有多个动脉瘤(34.37%)。大多数非裔美国患者有多个动脉瘤(28 名中有 25 名[89.3%])。大多数动脉瘤(n = 43 [87.75%])直径为 3 毫米或以下。在前循环或后循环中发现的动脉瘤在大小上无显著差异(p = 0.22)。同样,年龄、性别、种族、基因型或动脉瘤数量与大小无关。24/32 名患者(75%)有随访 MRA。除了 2 个动脉瘤(n = 2/38 [5.3%])外,其余动脉瘤在大小和形态上均保持稳定。2 名多发性颅内动脉瘤患者的动脉瘤大小出现间隔进展(n = 2/11 [18.2%])。

结论

在儿科 SCD 患者中,UIAs 的发生率高于先前报道。这些动脉瘤表现出多发性、与成人脑动脉瘤不同的非典型解剖分布、双侧受累和非裔美国人中更高的患病率。尽管大多数动脉瘤保持稳定,但有些动脉瘤的大小出现了间隔增长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验