Al-Smadi Anas, Shokuhfar Tahaamin, Johnston Andrew, Alden Tord D, Bowman Robin, Shaibani Ali
Departments of1Radiology and.
2Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois.
J Neurosurg Pediatr. 2017 Dec;20(6):591-597. doi: 10.3171/2017.7.PEDS17161. Epub 2017 Sep 29.
Intraosseous cranial arteriovenous malformations (AVMs) are very rare, challenging entities. The authors report the case of an extracranial parietooccipital vascular lesion. A 12-year-old boy presented with accelerated growth of a right scalp lesion over a few months. Digital subtraction angiography showed a large, right parietooccipital intraosseous AVM with multiple complex arterial feeders. Treatment of these lesions is difficult and can necessitate a multidisciplinary approach. In the featured case, 6 embolization procedures were performed over 1 year, including both transarterial and transvenous approaches, followed by total resection. The authors describe what is thought to be the second case of an AVM originating in the cranial bones and the first case with successful multidisciplinary management.
颅内骨内动静脉畸形(AVM)非常罕见,是具有挑战性的病症。作者报告了一例颅外顶枕部血管病变的病例。一名12岁男孩在几个月内出现右头皮病变加速生长。数字减影血管造影显示一个大型的右顶枕部骨内AVM,有多个复杂的动脉供血支。这些病变的治疗很困难,可能需要多学科方法。在该病例中,在1年的时间里进行了6次栓塞手术,包括经动脉和经静脉途径,随后进行了全切除。作者描述了这被认为是第二例起源于颅骨的AVM病例,也是第一例成功进行多学科治疗的病例。