Suppr超能文献

儿童髓内肿瘤的管理

Management of intramedullary tumours in children.

作者信息

Lunardi P, Licastro G, Missori P, Ferrante L, Fortuna A

机构信息

Department of Neurological Sciences, Neurosurgery, University of Rome, La Sapienza, Italy.

出版信息

Acta Neurochir (Wien). 1993;120(1-2):59-65. doi: 10.1007/BF02001471.

Abstract

Clinical presentation, diagnosis, surgical technique and results of 25 cases of intramedullary tumours in patients under 16 years of age are analyzed. Pre-operative spinal deformity was present in 9 patients. Surgery was performed in all. After multilaminectomy with preservation of the intervertebral joints, total removal of the lesion was achieved in 11 patients and subtotal removal in 14 others. After surgery, external immobilization lasting an average period of 5 years was instituted in all patients. Postoperative radiation therapy was performed in 11 cases (5 "high grade" astrocytomas, 5 ependymomas, 1 glioblastoma). There were 11 recurrences: 4 of which (2 ependymomas and 2 "low grade" astrocytomas) were treated surgically, 7 (5 "high grade" astrocytomas, 1 glioblastoma, 1 oligodendroglioma) with palliative radiation treatment. Six patients eventually developed postlaminectomy spinal deformities as diagnosed roentgenographically 6 to 50 months postoperatively. Of the 16 patients still alive, 7 did not present relevant neurological deficit, 1 presented a monoparesis, while the other 8 presented invalidating deficits. Surgical treatment did not differ from that employed in the intramedullary tumours in the adult: radical resection is indeed the optimal therapeutic origin. The risk of radiation therapy are greater in children: it is crucial to limit radiation therapy to only some histotypes. The incidence of spinal column deformity after multilevel laminectomy is greater in young patients. It is advisable to implement prevention of spinal deformities by postoperative external immobilization and constant follow-up so as to detect early changes of spinal stability.

摘要

分析了25例16岁以下患者髓内肿瘤的临床表现、诊断、手术技术及结果。9例患者术前存在脊柱畸形。所有患者均接受了手术。在保留椎间关节的情况下进行多节段椎板切除术后,11例患者实现了病变的全切,另外14例为次全切。术后所有患者均进行了平均为期5年的外固定。11例患者(5例“高级别”星形细胞瘤、5例室管膜瘤、1例胶质母细胞瘤)接受了术后放疗。有11例复发:其中4例(2例室管膜瘤和2例“低级别”星形细胞瘤)接受了手术治疗,7例(5例“高级别”星形细胞瘤、1例胶质母细胞瘤、1例少突胶质细胞瘤)接受了姑息性放疗。6例患者最终出现了椎板切除术后脊柱畸形,术后6至50个月经X线检查确诊。在16例存活患者中,7例无相关神经功能缺损,1例出现单瘫,另外8例出现致残性缺损。手术治疗与成人髓内肿瘤的治疗方法无异:根治性切除确实是最佳治疗方法。儿童放疗风险更大:将放疗仅限于某些组织学类型至关重要。年轻患者多节段椎板切除术后脊柱畸形的发生率更高。建议通过术后外固定和持续随访来预防脊柱畸形,以便早期发现脊柱稳定性的变化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验