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1型神经纤维瘤病患者丛状神经纤维瘤所致脊髓压迫症的外科治疗

Surgical management of spinal cord compression from plexiform neurofibromas in patients with neurofibromatosis 1.

作者信息

Pollack I F, Colak A, Fitz C, Wiener E, Moreland M, Mulvihill J J

机构信息

Department of Neurosurgery, Children's Hospital of Pittsburgh, Pennsylvania 15213, USA.

出版信息

Neurosurgery. 1998 Aug;43(2):248-55; discussion 255-6. doi: 10.1097/00006123-199808000-00038.

Abstract

OBJECTIVE

Plexiform neurofibromas with sizable intraspinal extensions and resultant spinal cord compromise pose challenging management problems, because these lesions may involve multiple nerves and engulf adjacent vascular and visceral structures. In this report, we review our experience with the surgical treatment of these lesions.

METHODS

Patients were identified by a detailed review of hospital medical records and the database of our multidisciplinary neurofibromatosis clinic. Ten patients had large plexiform neurofibromas that extended intraspinally, producing a combination of myelopathy and radiculopathy. Two patients exhibited single-level intraspinal growth, and eight showed multilevel involvement. Four patients showed bilateral plexiform neurofibromatous growth intraspinally, with "hourglass" compression of the spinal cord. Operative approaches and outcomes were reviewed in detail.

RESULTS

Gross total resection of the symptomatic intraspinal tumor component was achieved for nine patients. The management of the extraspinal component was individualized, depending on the pattern and extent of involvement of the surrounding structures. Nine patients experienced complete recovery of neurological function postoperatively; the remaining patient demonstrated significant functional improvement. With a median follow-up period of 4 years, only one patient has developed recurrent intraspinal compression, in this case from tumor involvement by the same plexiform lesion at a lower spinal level. Two patients treated early in the series using standard laminectomy approaches developed significant kyphotic deformities, necessitating subsequent fusion. Based on these initial results, osteoplastic laminotomy techniques were used in the last five cases, allowing anatomic reconstruction of the involved levels; none of these latter patients has developed significant kyphosis, with a median follow-up period of 3 years.

CONCLUSION

Radical resection of intraspinal tumor components in patients with neurofibromatosis 1 and large plexiform neurofibromas can help to preserve excellent neurological function. Technical factors in the management of these lesions are presented.

摘要

目的

伴有较大脊髓内延伸且导致脊髓受压的丛状神经纤维瘤带来了具有挑战性的管理问题,因为这些病变可能累及多条神经并包绕相邻的血管和内脏结构。在本报告中,我们回顾了我们对这些病变进行手术治疗的经验。

方法

通过详细查阅医院病历和我们多学科神经纤维瘤病诊所的数据库来确定患者。10例患者患有延伸至脊髓内的大型丛状神经纤维瘤,产生了脊髓病和神经根病的综合症状。2例患者表现为单节段脊髓内生长,8例表现为多节段受累。4例患者脊髓内呈双侧丛状神经纤维瘤生长,对脊髓造成“沙漏样”压迫。详细回顾了手术入路和结果。

结果

9例患者实现了有症状的脊髓内肿瘤成分的大体全切。脊髓外成分的处理根据周围结构受累的模式和范围进行个体化处理。9例患者术后神经功能完全恢复;其余1例患者功能有显著改善。中位随访期为4年,只有1例患者出现了复发性脊髓压迫,此次是同一丛状病变在较低脊髓节段累及肿瘤。该系列早期采用标准椎板切除术治疗的2例患者出现了明显的后凸畸形,需要随后进行融合手术。基于这些初步结果,后5例患者采用了骨成形性椎板切开术技术,实现了受累节段的解剖重建;这些患者中位随访期为3年,均未出现明显的后凸畸形。

结论

对1型神经纤维瘤病和大型丛状神经纤维瘤患者的脊髓内肿瘤成分进行根治性切除有助于保留良好的神经功能。本文介绍了这些病变管理中的技术因素。

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