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小儿颅外脊副神经神经鞘瘤:1例极其罕见的病例报告

Paediatric Extracranial Spinal Accessory Nerve Schwannoma: An Extremely Rare Case Report.

作者信息

Chakravarti Arunabha, Garg Sunil, Bhargava Rahul

机构信息

Professor, Department of Otorhinolaryngology- Head & Neck Surgery, Lady Hardinge Medical College & Associated Hospitals , New Delhi, India .

Senior Resident, Department of Otorhinolaryngology- Head & Neck Surgery, Lady Hardinge Medical College & Associated Hospitals , New Delhi, India .

出版信息

J Clin Diagn Res. 2016 Jul;10(7):MD01-2. doi: 10.7860/JCDR/2016/19373.8171. Epub 2016 Jul 1.

Abstract

Schwannoma in head and neck region are quiet common and generally arise from last four cranial nerves. Spinal accessory nerve involvement is very rare. We are hereby presenting an extremely rare case of paediatric XI nerve schwannoma hitherto unreported in English medical literature till date.

摘要

头颈部的神经鞘瘤较为常见,通常起源于最后四对脑神经。副神经受累极为罕见。我们在此报告一例极其罕见的小儿第十一脑神经神经鞘瘤,迄今为止英文医学文献中尚未有过报道。

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本文引用的文献

1
Imaging findings of neurogenic tumours in the head and neck region.头颈部神经源性肿瘤的影像学表现。
Dentomaxillofac Radiol. 2012 Jan;41(1):18-23. doi: 10.1259/dmfr/81000210. Epub 2011 Nov 10.
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Head and neck schwannomas--a 10 year review.头颈部神经鞘瘤——十年回顾
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Paediatric neck masses--a diagnostic dilemma.小儿颈部肿块——诊断难题
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Benign solitary Schwannomas (neurilemomas).良性孤立性施万瘤(神经鞘瘤)。
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