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本文引用的文献

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Malignant Peripheral Nerve Sheath Tumor: molecular pathogenesis and current management considerations.恶性周围神经鞘膜瘤：分子发病机制及当前治疗考量
J Surg Oncol. 2008 Mar 15;97(4):340-9. doi: 10.1002/jso.20971.
2
The 2007 WHO classification of tumours of the central nervous system.2007年世界卫生组织中枢神经系统肿瘤分类
Acta Neuropathol. 2007 Aug;114(2):97-109. doi: 10.1007/s00401-007-0243-4. Epub 2007 Jul 6.
3
Malignant peripheral nerve sheath tumors: prognostic factors and survival in a series of patients treated at a single institution.恶性周围神经鞘膜瘤：单机构治疗的一系列患者的预后因素及生存情况
Cancer. 2006 Sep 1;107(5):1065-74. doi: 10.1002/cncr.22098.
4
Pediatric malignant peripheral nerve sheath tumor: the Italian and German soft tissue sarcoma cooperative group.小儿恶性外周神经鞘瘤：意大利和德国软组织肉瘤协作组
J Clin Oncol. 2005 Nov 20;23(33):8422-30. doi: 10.1200/JCO.2005.01.4886.
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Peripheral nerve tumors: management strategies and molecular insights.周围神经肿瘤：管理策略与分子见解
J Neurooncol. 2004 Aug-Sep;69(1-3):335-49. doi: 10.1023/b:neon.0000041891.39474.cb.
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Malignant peripheral nerve sheath tumors.恶性外周神经鞘瘤
Neurosurg Clin N Am. 2004 Apr;15(2):203-16. doi: 10.1016/j.nec.2004.02.004.
7
Malignant peripheral nerve sheath tumor: the clinical spectrum and outcome of treatment.恶性周围神经鞘膜瘤：临床谱及治疗结果
Neurology. 2003 Sep 9;61(5):696-8. doi: 10.1212/01.wnl.0000078813.05925.2c.
8
Evaluation of F18-deoxyglucose positron emission tomography (FDG-PET) to assess the nature of neurogenic tumours.评估F18-脱氧葡萄糖正电子发射断层扫描（FDG-PET）以确定神经源性肿瘤的性质。
Eur J Surg Oncol. 2003 Aug;29(6):536-41. doi: 10.1016/s0748-7983(03)00055-6.
9
Malignant peripheral nerve sheath tumor.恶性外周神经鞘瘤。
Radiographics. 2003 May-Jun;23(3):790-4. doi: 10.1148/rg.233025153.
10
Histopathologic type: an independent prognostic factor in primary soft tissue sarcoma of the extremity?组织病理学类型：肢体原发性软组织肉瘤的独立预后因素？
Ann Surg Oncol. 2003 May;10(4):432-40. doi: 10.1245/aso.2003.05.014.

原发性脊柱旁恶性周围神经鞘瘤。

Primary paraspinal malignant peripheral nerve sheath tumor.

作者信息

Kim Kyoung-Tae, Park Yong-Suk, Kwon Jeong-Taik, Kim Young-Baeg

机构信息

Department of Neurosurgery, College of Medicine, Chung-Ang University, Seoul, Korea.

出版信息

J Korean Neurosurg Soc. 2008 Aug;44(2):91-4. doi: 10.3340/jkns.2008.44.2.91. Epub 2008 Aug 30.

DOI:10.3340/jkns.2008.44.2.91
PMID:19096700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2588335/
Abstract

Malignant peripheral nerve sheath tumors (MPNSTs) are very rare tumors. We experienced a case of MPNST in the cervical paraspinal space which was not associated with neurofibromatosis. The tumor located in left C6-7 foramen and compressed C7 root. The tumor was removed through the occipital triangle. We report a case of the primary cerivcal MPNST in a patient who did not have neurofibromatosis-1.

摘要

恶性外周神经鞘瘤（MPNSTs）是非常罕见的肿瘤。我们遇到一例位于颈椎旁间隙的MPNST，该病例与神经纤维瘤病无关。肿瘤位于左侧C6 - 7椎间孔并压迫C7神经根。通过枕三角将肿瘤切除。我们报告一例无神经纤维瘤病1型患者的原发性颈椎MPNST病例。