Kolias Angelos G, Pal Debasish, Shivane Aditya, Ismail Azzam, Tyagi Atul K
Department of Neurosurgery, Leeds General Infirmary, Great George Street, Leeds, West Yorkshire, LS1 3EX, United Kingdom.
Clin Neurol Neurosurg. 2009 Nov;111(9):784-8. doi: 10.1016/j.clineuro.2009.07.002. Epub 2009 Aug 3.
Cavernous malformations are vascular lesions which can occur throughout the entire neuraxis. This term is synonymous to cavernous angioma, cavernous haemangioma, and cavernoma. They comprise of closely packed, capillary-like vascular channels, without intervening neural tissue. MR imaging is currently the study of choice for the diagnosis of cavernous malformations as they are considered angiographically occult lesions. Intramedullary location represents only 3-5% of all central nervous system cavernous malformations, with the majority of them being supratentorial. Only 10% of the intramedullary cavernous malformations present in the paediatric population. As the natural history of these lesions is not well known, the debate on the optimal management of them is still ongoing. Here we describe the case of a 14-year-old male with progression of symptoms over an 18 months period, which necessitated microsurgical removal of a T9 intramedullary cavernous malformation.
海绵状血管畸形是一种可发生于整个神经轴的血管病变。该术语与海绵状血管瘤、海绵状血管瘤和海绵状瘤同义。它们由紧密排列的、类似毛细血管的血管通道组成,其间无神经组织。目前,磁共振成像(MR成像)是诊断海绵状血管畸形的首选检查方法,因为它们在血管造影上被视为隐匿性病变。髓内病变仅占所有中枢神经系统海绵状血管畸形的3%-5%,其中大多数位于幕上。小儿人群中仅10%的海绵状血管畸形位于髓内。由于这些病变的自然病史尚不清楚,关于其最佳治疗方法的争论仍在继续。在此,我们描述一例14岁男性患者,其症状在18个月内逐渐进展,因此需要显微手术切除T9节段的髓内海绵状血管畸形。