Zenonos Georgios, Jamil Osama, Governale Lance S, Jernigan Sarah, Hedequist Daniel, Proctor Mark R
Department of Neurological Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
J Neurosurg Pediatr. 2012 Mar;9(3):305-15. doi: 10.3171/2011.12.PEDS11253.
Spinal aneurysmal bone cysts (ABCs) constitute a rare and clinically challenging disease, primarily affecting the pediatric population. Information regarding the management of spinal ABCs remains sparse. In this study the authors review their experience with spinal ABCs at Children's Hospital Boston.
The medical records of all patients treated surgically for primary spinal ABCs between January 1998 and July 2010 were retrospectively reviewed.
Fourteen cases were identified (6 males and 8 females, ages 5-19 years old). The ABCs were located throughout the spine, with an equal number in the thoracic and lumbar spine, and rarely in the cervical spine. The majority of patients presented with back pain, but neurological deficits and spinal deformity were common. A variety of radiographic techniques were used to establish the diagnosis, including needle biopsy. Preoperative selective arterial embolization was performed in 7 cases (50%), and the majority of cases required spinal instrumentation along with resection. Mean follow-up was 55.9 months (range 15-154 months) after initial intervention. Two ABCs recurred (14%), at 9 months and 8 years after incomplete initial resection, and the patients underwent reoperation. Complete resection was ultimately achieved in all cases. All patients were asymptomatic and neurologically intact at their last follow-up evaluation, and showed no evidence of deformity or recurrence on imaging.
Computed tomography and MR imaging are adequate for an initial evaluation of spinal ABCs, although solid variants can present a diagnostic challenge. Given the high rates of recurrence with residual disease, complete obliteration of the lesion should be the goal of treatment. Preoperative embolization is often performed, although in the authors' opinion the degree of bleeding tends not to support its routine use. Long-term follow-up is warranted as recurrences can occur years after initial intervention. However, gross-total excision in conjunction with spinal stabilization, as needed, usually provides cure of the ABC and excellent long-term spinal alignment.
脊柱动脉瘤样骨囊肿(ABCs)是一种罕见且临床治疗具有挑战性的疾病,主要影响儿童群体。关于脊柱ABCs治疗的信息仍然匮乏。在本研究中,作者回顾了他们在波士顿儿童医院治疗脊柱ABCs的经验。
对1998年1月至2010年7月期间因原发性脊柱ABCs接受手术治疗的所有患者的病历进行回顾性分析。
共确定14例患者(男6例,女8例,年龄5 - 19岁)。ABCs位于整个脊柱,胸椎和腰椎数量相等,颈椎少见。大多数患者表现为背痛,但神经功能缺损和脊柱畸形也很常见。采用多种影像学技术进行诊断,包括穿刺活检。7例(50%)患者术前行选择性动脉栓塞,大多数病例需要在切除的同时进行脊柱内固定。首次干预后平均随访55.9个月(范围15 - 154个月)。2例ABCs复发(14%),分别在初次不完全切除后9个月和8年,患者接受了再次手术。最终所有病例均实现了完全切除。所有患者在最后一次随访评估时均无症状且神经功能完好,影像学检查未显示畸形或复发迹象。
计算机断层扫描和磁共振成像足以对脊柱ABCs进行初步评估,尽管实体变体可能带来诊断挑战。鉴于残留病灶复发率高,彻底清除病灶应是治疗目标。虽然作者认为出血程度往往不支持常规使用,但术前栓塞仍经常进行。由于复发可能在初次干预数年之后发生,因此需要长期随访。然而,根据需要进行全切除并结合脊柱稳定术通常可治愈ABCs,并实现良好的长期脊柱对线。