Thomas Matthew, Hoening Dirk, Stauffer John, Atkins Bethany
Pediatrics and Child Health, Lake Erie College of Osteopathic Medicine, Bradenton, USA.
General Surgery, Lake Erie College of Osteopathic Medicine, Bradenton, USA.
Cureus. 2025 Apr 5;17(4):e81765. doi: 10.7759/cureus.81765. eCollection 2025 Apr.
Arteriovenous malformations (AVMs) in the pediatric population are rare but represent a critical cause of spontaneous intracranial hemorrhage. Here we present the case of an 11-year-old boy who developed acute-onset left-sided weakness, slurred speech, and transient hemiparesis. While initial laboratory findings were unremarkable, brain magnetic resonance imaging revealed a large right cerebral AVM. Cerebral angiography confirmed this finding, showing a Spetzler-Martin grade V AVM, supplied by the middle, anterior, and posterior cerebral arteries. The patient was treated using a multimodal approach, including embolization and encephaloduroarteriosynangiosis (EDAS). Postoperatively, he experienced transient worsening of hemiparesis of unknown etiology, which gradually improved. Long-term follow-up demonstrated improved motor function with persistent mild left-sided weakness. This case highlights the significance of multimodal management in high-grade pediatric AVMs. This particular includes the utility of EDAS, originally developed for moyamoya disease, in mitigating ischemia by promoting collateral neovascularization and thus improving neurological symptoms.
小儿动静脉畸形(AVM)较为罕见,但却是自发性颅内出血的一个关键原因。在此,我们报告一例11岁男孩,他出现急性发作的左侧肢体无力、言语含糊和短暂性偏瘫。虽然最初的实验室检查结果无异常,但脑部磁共振成像显示右侧大脑有一个大型AVM。脑血管造影证实了这一发现,显示为Spetzler-Martin V级AVM,由大脑中动脉、前动脉和后动脉供血。该患者采用了包括栓塞和脑-硬脑膜-动脉血管融合术(EDAS)在内的多模式治疗方法。术后,他出现了病因不明的偏瘫短暂加重,随后逐渐改善。长期随访显示运动功能有所改善,但仍持续存在轻度左侧肢体无力。本病例突出了多模式管理在高级别小儿AVM中的重要性。这尤其包括最初为烟雾病开发的EDAS在通过促进侧支新生血管形成减轻缺血从而改善神经症状方面的效用。