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本文引用的文献

1
Asymptomatic schwannoma of the oculomotor nerve: case report.动眼神经无症状性神经鞘瘤:病例报告
J Clin Neurosci. 2000 Sep;7(5):458-60. doi: 10.1054/jocn.1999.0240.
2
Third nerve palsies.动眼神经麻痹
Semin Neurol. 2000;20(1):55-74. doi: 10.1055/s-2000-6833.
3
Isolated oculomotor nerve palsy in lymphoma.淋巴瘤中的孤立性动眼神经麻痹
Neurol Res. 2000 Jun;22(4):347-8. doi: 10.1080/01616412.2000.11740681.
4
Schwannoma of the oculomotor nerve: a case report with consideration of the surgical treatment.动眼神经鞘瘤:一例报告并探讨手术治疗
Neurosurgery. 1999 Sep;45(3):630-3; discussion 633-4. doi: 10.1097/00006123-199909000-00039.
5
Benign triton tumor of the trigeminal nerve.三叉神经良性蝾螈瘤
Childs Nerv Syst. 1999 Mar;15(2-3):140-4. doi: 10.1007/s003810050353.
6
Isolated oculomotor nerve palsy: an unusual presentation of glioblastoma multiforme. Case report and review of the literature.孤立性动眼神经麻痹:多形性胶质母细胞瘤的一种不寻常表现。病例报告及文献复习。
J Neurooncol. 1999 Jan;41(1):77-80. doi: 10.1023/a:1006185421774.
7
Third, fourth, and sixth cranial nerve palsies.第三、第四和第六颅神经麻痹。
Curr Opin Ophthalmol. 1997 Dec;8(6):45-51. doi: 10.1097/00055735-199712000-00008.
8
Surgically created fourth-third cranial nerve communication: temporary success in a child with bilateral third nerve hamartomas. Case report.
J Neurosurg. 1999 Mar;90(3):542-5. doi: 10.3171/jns.1999.90.3.0542.
9
Malignant meningioma of the oculomotor nerve without dural attachment. Case report and review of the literature.
J Neurosurg. 1998 Jun;88(6):1104-6. doi: 10.3171/jns.1998.88.6.1104.
10
Primary intracranial germ cell tumors: clinicopathologic review of 32 cases.原发性颅内生殖细胞肿瘤:32例临床病理分析
Pediatr Pathol Lab Med. 1997 Sep-Oct;17(5):713-27.

动眼神经畸胎瘤

Oculomotor nerve teratoma.

作者信息

Moore K R

机构信息

Department of Radiology, Section of Neuroradiology, University of Utah School of Medicine, Salt Lake City 84106, USA.

出版信息

AJNR Am J Neuroradiol. 2001 Sep;22(8):1566-9.

PMID:11559507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7974582/
Abstract

The case of a rare, mature teratoma of the oculomotor nerve manifesting as an interpeduncular cistern mass is presented. A basilar tip aneurysm initially was suspected on the basis of lesion location and MR imaging appearance. Subsequent CT and catheter angiography studies were atypical for aneurysm, leading to surgical biopsy. Pathologic analysis revealed a well-circumscribed mass composed of mature representatives of all three major cell lines characteristic of mature teratoma. The imaging findings are described, and a brief literature review is provided.

摘要

本文报告一例罕见的动眼神经成熟畸胎瘤,表现为脚间池肿块。基于病变位置和磁共振成像表现,最初怀疑为基底动脉尖部动脉瘤。随后的计算机断层扫描和导管血管造影检查结果不典型,遂进行手术活检。病理分析显示,肿块边界清晰,由成熟畸胎瘤特征性的所有三种主要细胞系的成熟成分组成。文中描述了影像学表现,并提供了简要的文献综述。