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不同部位内听神经鞘瘤的临床表现-系统综述。

Different clinical presentation of intralabyrinthine schwannomas - a systematic review.

机构信息

Universidade Federal de São Paulo (UNIFESP), Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo, SP, Brazil.

Universidade Federal de São Paulo (UNIFESP), Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo, SP, Brazil.

出版信息

Braz J Otorhinolaryngol. 2019 Jan-Feb;85(1):111-120. doi: 10.1016/j.bjorl.2018.05.007. Epub 2018 Jun 21.

DOI:10.1016/j.bjorl.2018.05.007
PMID:29980446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9442840/
Abstract

INTRODUCTION

Intralabyrinthine schwannoma is a rare, benign tumor that affects the most terminal portions of the vestibular and cochlear nerves. This tumor can be classified into 10 subtypes, according to its inner ear location.

OBJECTIVE

To carry out a comprehensive review of the most frequent auditory manifestations secondary to the intralabyrinthine schwannoma, describing the possible underlying pathophysiological mechanisms.

METHODS

Systematic review of the literature until October 2017 using the PubMed, Web of Science and Scopus databases. The inclusion criteria were clinical manifestations of the intralabyrinthine schwannoma. Three researchers independently assessed the articles and extracted relevant information. The description of a case of an intravestibular subtype intralabyrinthine schwannoma with multiple forms of clinical presentations was used as an example.

RESULTS

Twenty-seven studies met our inclusion criteria. The most common intralabyrinthine schwannoma subtype was the intracochlear, followed by the intravestibular type. All the cases demonstrated hearing loss, usually progressive hearing loss.

CONCLUSION

The diagnosis of intralabyrinthine schwannomas is based on high-resolution magnetic resonance imaging and should be included in the differential diagnosis of patients with vestibulocochlear complaints. Although there are approximately 600 cases in the literature, we still lack a detailed description of the clinical evolution of the patients, correlating it with MRI findings of temporal bones and tumor subtype.

摘要

简介

内淋巴囊神经鞘瘤是一种罕见的良性肿瘤,影响前庭和耳蜗神经的最末端部分。根据其内耳位置,这种肿瘤可分为 10 个亚型。

目的

对内淋巴囊神经鞘瘤引起的最常见听觉表现进行全面回顾,描述可能的潜在病理生理机制。

方法

使用 PubMed、Web of Science 和 Scopus 数据库对 2017 年 10 月之前的文献进行系统回顾。纳入标准为内淋巴囊神经鞘瘤的临床表现。三名研究人员独立评估文章并提取相关信息。以一例前庭型内淋巴囊神经鞘瘤的多种临床表现为例进行描述。

结果

符合纳入标准的研究有 27 项。最常见的内淋巴囊神经鞘瘤亚型是耳蜗内型,其次是前庭内型。所有病例均表现为听力损失,通常为进行性听力损失。

结论

内淋巴囊神经鞘瘤的诊断基于高分辨率磁共振成像,应纳入前庭耳蜗症状患者的鉴别诊断。尽管文献中有大约 600 例病例,但我们仍然缺乏对患者临床演变的详细描述,并将其与颞骨的 MRI 发现和肿瘤亚型相关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/77d71e7c01b5/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/ae7ef73d4967/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/8b03d15bc1e9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/ab20a90da495/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/60593a5843a5/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/84330ea1ca4b/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/19893a2a5b73/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/77d71e7c01b5/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/ae7ef73d4967/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/8b03d15bc1e9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/ab20a90da495/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/60593a5843a5/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/84330ea1ca4b/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/19893a2a5b73/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a9/9442840/77d71e7c01b5/gr7.jpg

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Intralabyrinthine schwannomas: imaging diagnosis and classification.内淋巴囊神经鞘瘤:影像学诊断与分类。
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