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赫米巴斯综合征:颅内副神经节瘤的一种不寻常表现。

Hemibase syndrome: an unusual presentation of intracranial paraganglioma.

作者信息

Prabhakar S, Sawhney I M, Chopra J S, Kak V K, Banerjee A K

出版信息

Surg Neurol. 1984 Jul;22(1):39-42. doi: 10.1016/0090-3019(84)90226-x.

Abstract

A case of paraganglioma of parasellar origin in a 7-year-old girl is described. She presented with hemibase syndrome with involvement of a majority of the left cranial nerves. Three times in the past 2 years she had recurrent ophthalmoplegia with complete recovery. She was treated surgically and with postoperative radiotherapy. The site of origin of this paraganglioma as well as the clinical presentation are uncommon features in this case.

摘要

本文描述了一名7岁女孩的鞍旁副神经节瘤病例。她表现为半侧基底综合征,累及多数左侧颅神经。在过去2年中,她曾3次出现复发性眼肌麻痹,但均完全恢复。她接受了手术治疗及术后放疗。该副神经节瘤的起源部位及临床表现为本病例的罕见特征。

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引用本文的文献

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Suprasellar paraganglioma: a case report and review of the literature.鞍上副神经节瘤:一例病例报告及文献复习
Neuroradiology. 2005 Oct;47(10):753-7. doi: 10.1007/s00234-005-1422-4. Epub 2005 Jul 27.
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Cauda equina paraganglioma with subsequent intracranial and intraspinal metastases.
Acta Neurochir (Wien). 1996;138(4):475-9. doi: 10.1007/BF01420312.

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