Nagib M G, O'Fallon M T
Neurosurgical Associates, Ltd., Minneapolis, Minn., USA.
Pediatr Neurosurg. 1997 Jan;26(1):2-7. doi: 10.1159/000121154.
Myxopapillary ependymoma of the conus medullaris and filum terminale is a relatively common spinal intradural neoplasm in adulthood. However, only a reported 8-12% of such tumors affect this site in children, and the ideal management remains controversial. Three children with myxopapillary ependymomas of the conus medullaris and filum terminale were treated by the author over a 2-year period with an at least 24-month follow-up. These children, ages 7, 8 and 13 years, included 1 male and 2 females. Their salient presentation was an acute exacerbation of chronic lower back pain. The duration of symptoms prior to diagnosis ranged from 16 to 18 months. A preoperative MRI, with and without contrast, was available for every case. All children underwent replacement laminoplasty with gross total tumor resection. Somatosensory evoked potentials were used in all surgeries. An early postoperative MRI of the entire neural axis was available for all cases. No permanent complications were noted. Self-catheterization for 6 weeks was required in 1 child with preoperative urinary incontinence. One child received radiation therapy following a recurrence. Clinical and surgical results were compared to the only 2 other reported series (11 patients) addressing this type of tumor in children. Based on this review, the authors propose that: (1) unexplained and intractable lumbar pain in childhood should be thoroughly investigated with an MRI scan: (2) the gross feature of myxopapillary ependymoma allowing for complete resectability appears to be the key prognostic factor; (3) radiotherapy appeared to have no proven value in completely resected tumors in children; (4) postoperative baseline MRI and regular sequential imaging studies are essential for long-term follow-up, and (5) replacement laminoplasties may be of value in preventing future spinal deformities, musculoskeletal pain and allowing for an 'easier' resection in the event of a recurrence.
圆锥和终丝的黏液乳头型室管膜瘤是成人相对常见的脊髓硬膜内肿瘤。然而,据报道,此类肿瘤在儿童中仅有8% - 12%发生于此部位,且理想的治疗方法仍存在争议。作者在2年时间里治疗了3例圆锥和终丝黏液乳头型室管膜瘤患儿,并进行了至少24个月的随访。这些患儿年龄分别为7岁、8岁和13岁,包括1名男性和2名女性。他们的突出表现是慢性下背痛急性加重。诊断前症状持续时间为16至18个月。每例均有术前增强和未增强的MRI检查。所有患儿均接受了全肿瘤切除的替代椎板成形术。所有手术均使用体感诱发电位。所有病例术后均有早期全神经轴MRI检查。未发现永久性并发症。1例术前有尿失禁的患儿术后需自行导尿6周。1例患儿复发后接受了放疗。将临床和手术结果与另外仅有的2篇报道的系列研究(共11例患者)进行了比较,该系列研究涉及儿童此类肿瘤。基于此综述,作者提出:(1) 儿童不明原因的顽固性腰痛应通过MRI扫描进行全面检查;(2) 黏液乳头型室管膜瘤允许完整切除的大体特征似乎是关键的预后因素;(3) 放疗在儿童完全切除的肿瘤中似乎没有已证实的价值;(4) 术后基线MRI和定期的序贯影像学检查对长期随访至关重要;(5) 替代椎板成形术可能有助于预防未来的脊柱畸形、肌肉骨骼疼痛,并在复发时便于进行“更轻松”的切除。