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本文引用的文献

1
Unilateral double vestibular schwannoma.单侧双前庭神经鞘瘤
Otol Neurotol. 2005 Nov;26(6):1241-2. doi: 10.1097/01.mao.0000194894.10850.04.
2
Multiple unilateral schwannomas: segmental neurofibromatosis type 2 or schwannomatosis?多发性单侧神经鞘瘤:2型节段性神经纤维瘤病还是神经鞘瘤病?
Br J Dermatol. 2003 Apr;148(4):804-9. doi: 10.1046/j.1365-2133.2003.05249.x.
3
On the myth of the glial/schwann junction (Obersteiner-Redlich zone): origin of vestibular nerve schwannomas.关于胶质/施万细胞连接(奥伯施泰纳-雷德利希区)的神话:前庭神经鞘瘤的起源
Otol Neurotol. 2003 Jan;24(1):1. doi: 10.1097/00129492-200301000-00001.
4
A clinical study of patients with multiple isolated neurofibromas.多发性孤立性神经纤维瘤患者的临床研究。
J Med Genet. 2001 Jul;38(7):485-8. doi: 10.1136/jmg.38.7.485.
5
Nerve origin of the acoustic neuroma.听神经瘤的神经起源。
J Laryngol Otol. 2001 May;115(5):376-9. doi: 10.1258/0022215011907910.
6
Neurofibromatosis type 2.2型神经纤维瘤病
J Med Genet. 2000 Dec;37(12):897-904. doi: 10.1136/jmg.37.12.897.
7
MRI screening for acoustic neuroma: a comparison of fast spin echo and contrast enhanced imaging in 1233 patients.磁共振成像筛查听神经瘤:1233例患者快速自旋回波与对比增强成像的比较
Br J Radiol. 2000 Mar;73(867):242-7. doi: 10.1259/bjr.73.867.10817038.
8
Asymptomatic acoustic neurilemoma.
Arch Otolaryngol. 1970 Feb;91(2):117-24. doi: 10.1001/archotol.1970.00770040187003.
9
Relative frequency of inferior vestibular schwannoma.
Arch Otolaryngol Head Neck Surg. 1986 Feb;112(2):190-4. doi: 10.1001/archotol.1986.03780020070016.
10
[Origin of acoustic neuroma].[听神经瘤的起源]
Ann Otolaryngol Chir Cervicofac. 1986;103(7):475-7.

单侧散发性前庭神经鞘瘤的双重定位

Double localization of a unilateral sporadic vestibular schwannoma.

作者信息

Barbara M, Ronchetti F, Manni V, Monini S

机构信息

Department of Sensory Organs, Otorhinolaryngologic Unit, II Medical School, "La Sapienza" University, Rome, Italy.

出版信息

Acta Otorhinolaryngol Ital. 2008 Feb;28(1):34-7.

PMID:18533554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2640061/
Abstract

Vestibular schwannoma may present as a sporadic or genetically-based multi-localized benign neoplasm of the internal auditory canal and/or cerebello-pontine angle region. Multiple localization is generally regarded as genetic in origin and often affects the stato-acoustic bundle on both sides. A case of double vestibular schwannoma localized on the same stato-acoustic bundle is presented. After removal, slight histological differences were found between the two separate masses. From these findings, the possibility of a unilateral multiple localization of a vestibular schwannoma is considered plausible within the range of clinical presentation, with negative genetic features. Whether these individual masses might have an autonomous origin or a different growth pattern remains to be fully elucidated.

摘要

前庭神经鞘瘤可能表现为内耳道和/或桥小脑角区域的散发性或基于遗传的多灶性良性肿瘤。多灶性通常被认为起源于遗传,且常双侧累及听神经束。本文报告一例双侧前庭神经鞘瘤位于同一听神经束的病例。切除后,发现两个独立肿块之间存在轻微的组织学差异。基于这些发现,在前庭神经鞘瘤临床表现范围内,具有阴性遗传特征的单侧多灶性发生被认为是合理的。这些单个肿块是否可能有自主起源或不同的生长模式仍有待充分阐明。