Killeen Tim, Czaplinski Adam, Cesnulis Evaldas
Department of Neurosurgery, Swiss Neuro Institute , Klinik Hirslanden, Zurich , Switzerland.
Br J Neurosurg. 2014 Jun;28(3):340-6. doi: 10.3109/02688697.2013.841858. Epub 2013 Sep 27.
Purely extradural spinal cavernous malformations (ESCMs) are rare, but the number of cases reported seems to be increasing. A 44-year-old woman presented with progressive cervicothoracic back pain, lower limb paraesthesia and hypertonia. MRI showed a well-circumscribed, convex lesion in the T1-4 extradural space causing cord compression and encroaching into the left T2/3 neural foramen. Selective spinal angiography demonstrated a vascular blush at the T2/T3 level corresponding with the mass. A feeding vessel arising from the base of the T1 spinous process was identified and successfully catheterised, but embolisation was precluded by unfavourable anatomy of the posterior spinal artery. At hemilaminectomy, the lesion was found to be an ESCM. The patient went on to make a full recovery. We reviewed 71 cases of ESCM reported in the last decade. Incidence of ESCM is unclear; the largest case series reported on nine patients, but most published accounts were single case studies. Patients presented with back pain (33%), myelopathy (56%) and/or radiculopathy (39%). Onset of symptoms was usually insidious over months to years, but 30% presented with sudden-onset neurological symptoms, often due to spontaneous haemorrhage. Mean age at diagnosis was 44 (range, 2-74; SD, 19.6) years with a 1:1 sex ratio. Lesions were found at all levels except C1-C2, but a strong predilection for the dorsal thoracic spine (68%) was shown. The lesion extended into an intravertebral foramen in at least 24 cases (34%). MRI is the investigation of choice, and angiography of ESCM has rarely been described. Most (87%) were hypo- to isointense on T1 MRI while hyperintensity on T2 (91%) and avid (89%), usually homogenous gadolinium update was almost universal. Perilesional haemosiderin, characteristic of intracranial and intramedullary cavernous malformation was rarely seen. In many cases, meningioma or nerve sheath tumour was misdiagnosed prior to surgery. All patients underwent total (95%) or subtotal (5%) microsurgical resection with excellent results; all improved (23%) or recovered fully (77%) after surgery. Those who presented acutely did worse; 38% had residual deficits.
单纯硬膜外脊髓海绵状畸形(ESCMs)较为罕见,但报告的病例数量似乎在增加。一名44岁女性出现进行性颈胸背部疼痛、下肢感觉异常和张力亢进。MRI显示T1-4硬膜外间隙有一个边界清晰、凸形的病变,导致脊髓受压并侵入左侧T2/3神经孔。选择性脊髓血管造影显示T2/T3水平有与肿块相对应的血管造影剂充盈。发现一根供血血管发自T1棘突根部并成功插管,但由于脊髓后动脉解剖结构不利,无法进行栓塞。在半椎板切除术中,发现病变为ESCM。患者随后完全康复。我们回顾了过去十年中报告的71例ESCM病例。ESCM的发病率尚不清楚;最大的病例系列报道了9例患者,但大多数已发表报告为单病例研究。患者表现为背痛(33%)、脊髓病(56%)和/或神经根病(39%)。症状通常在数月至数年中隐匿起病,但30%的患者出现突发神经症状,通常是由于自发性出血。诊断时的平均年龄为44岁(范围2-74岁;标准差19.6),男女比例为1:1。除C1-C2外,各节段均发现病变,但以胸段脊柱背侧最为常见(68%)。至少24例(34%)病变延伸至椎间孔。MRI是首选检查方法,关于ESCM血管造影的描述很少。大多数(87%)在T1 MRI上呈低至等信号,而在T2上呈高信号(91%),且造影剂摄取活跃(89%),通常为均匀强化,几乎是普遍现象。病变周围很少见到颅内和髓内海绵状畸形特有的含铁血黄素。在许多病例中,术前误诊为脑膜瘤或神经鞘瘤。所有患者均接受了全切除(95%)或次全切除(5%)显微手术,效果良好;术后所有患者均有改善(23%)或完全康复(77%)。急性起病的患者预后较差;38%有残留神经功能缺损。