Development of moyamoya arteriopathy following treatment of intracranial tumors: clinical and radiographic characterization.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY
Journal of neurosurgery. Pediatrics Pub Date : 2024-05-03 Print Date: 2024-08-01 DOI:10.3171/2024.3.PEDS23479
Jong Seok Lee, Armide Storey, Arianna Lanpher, Edward R Smith
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引用次数: 0

Abstract

Objective: Moyamoya arteriopathy can develop in patients with brain tumors, particularly when associated with neurofibromatosis type 1 (NF1) or cranial irradiation. The present study aimed to analyze the clinical outcomes of moyamoya after brain tumor treatment and elucidate the effect of revascularization on brain tumors.

Methods: The authors retrospectively reviewed clinical and radiographic findings in 27 patients with brain tumors who developed moyamoya requiring revascularization surgery between January 1985 and June 2017 at a single institution. The long-term clinical and neuroimaging-based outcomes were analyzed.

Results: Among 27 patients, 22 patients underwent radiotherapy, and 12 patients had NF1. The mean ages at diagnosis of brain tumors and moyamoya were 4.4 years and 10.3 years, respectively. The mean interval between radiotherapy and moyamoya diagnosis was 4.0 years. The mean follow-up period after revascularization surgery was 8.5 years. Among 46 affected hemispheres in 27 patients, the patients who underwent radiotherapy (30 hemispheres in 22 patients) had a higher incidence of Suzuki stage 5 or 6 (20% [6/30] vs 0% [0/8]) and infarction (63.6% [14/22] vs 0% [0/5]) compared with patients without radiotherapy (8 hemispheres in 5 patients). After revascularization, stroke occurred in 4 patients, and 6 hemispheres showed Matsushima grade C, all of which occurred in patients with a history of radiotherapy. The residual brain tumors progressed in 4 of 21 patients (19%) after revascularization, comparable to the progression rates of brain tumors without revascularization in previous literature.

Conclusions: Patients with brain tumors can develop moyamoya that exhibits characteristic clinical and radiographic features of idiopathic MMD. Moyamoya associated with cranial irradiation has a higher incidence of stroke with less capacity for revascularization, requiring thorough evaluations and timely treatment. Revascularization does not appear to have any effect on the progression of existing brain tumors.

治疗颅内肿瘤后出现的莫亚莫亚动脉病变:临床和影像学特征。
目的:脑肿瘤患者,尤其是伴有神经纤维瘤病1型(NF1)或颅脑照射的患者,可能发生莫亚莫亚动脉病变。本研究旨在分析脑肿瘤治疗后莫亚莫亚动脉病变的临床结果,并阐明血管重建对脑肿瘤的影响:作者回顾性研究了一家机构在1985年1月至2017年6月期间27例发生moyamoya需要进行血管重建手术的脑肿瘤患者的临床和影像学结果。结果:在27名患者中,22名患者接受了放射治疗,12名患者患有NF1。脑肿瘤和moyamoya的平均诊断年龄分别为4.4岁和10.3岁。放疗与确诊莫亚莫亚病的平均间隔时间为 4.0 年。血管重建手术后的平均随访时间为 8.5 年。在 27 名患者的 46 个受影响半球中,接受放射治疗的患者(22 名患者的 30 个半球)与未接受放射治疗的患者(5 名患者的 8 个半球)相比,铃木 5 期或 6 期(20% [6/30] vs 0% [0/8])和脑梗死(63.6% [14/22] vs 0% [0/5])的发生率更高。血管重建后,4 名患者发生了中风,6 个半球显示松岛 C 级,所有这些都发生在有放疗史的患者身上。血管再通后,21 名患者中有 4 人(19%)的残余脑瘤出现进展,与之前文献中未进行血管再通的脑瘤进展率相当:结论:脑肿瘤患者也可能患上moyamoya,并表现出特发性MMD的临床和影像学特征。与头颅照射相关的莫亚莫亚症中风发病率较高,血管再通能力较弱,需要全面评估和及时治疗。血管再通似乎对现有脑肿瘤的进展没有任何影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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