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喉神经鞘瘤:一项系统评价

Laryngeal schwannoma: a systematic review.

作者信息

Wong Billy L K, Bathala S, Grant D

机构信息

Department of Otolaryngology, Head and Neck Surgery, Queen's Medical Centre, Nottingham University Hospitals NHS Trust, Derby Road, Nottingham, NG7 2UH, UK.

出版信息

Eur Arch Otorhinolaryngol. 2017 Jan;274(1):25-34. doi: 10.1007/s00405-016-4013-6. Epub 2016 Mar 28.

Abstract

A large proportion of schwannomas are found in the head and neck region. Schwannoma located within the larynx however is uncommon. The characteristic features, clinical presentations, treatment and the outcomes of patients with laryngeal schwannoma are therefore not clearly understood. The aim of this comprehensive review is to compile, analyze and present the details to develop a consensus and augment the available literature on laryngeal schwannoma. A comprehensive literature search on laryngeal schwannoma was performed on PUBMED/MEDLINE, EMBASE, CINAHL and Science Citation Index using MeSH words. A total of 55 patients were reviewed in this study. 40.7 % of the tumours arose from the aryepiglottic fold or arytenoids. Other areas where tumours were found included the false cord, true vocal cord, epiglottis, subglottis, piriform sinus and the post cricoid area. 64.9 % patients presented with dysphonia. Others typically present with multiple symptoms related to the mass effect and location of the tumour. All patients were managed surgically with different techniques and approaches. Majority of patients were alive with no residual disease. There were five recurrences and no mortality to date. Schwannoma within the larynx can present with a variety of symptoms. Surgical excision remained as the treatment of choice with good overall prognosis.

摘要

大部分神经鞘瘤位于头颈部区域。然而,位于喉内的神经鞘瘤并不常见。因此,喉神经鞘瘤患者的特征、临床表现、治疗方法及预后尚不清楚。这篇综述的目的是收集、分析并呈现相关细节,以达成共识并丰富有关喉神经鞘瘤的现有文献。使用医学主题词在PUBMED/MEDLINE、EMBASE、CINAHL和科学引文索引上对喉神经鞘瘤进行了全面的文献检索。本研究共纳入55例患者。40.7%的肿瘤起源于杓会厌襞或杓状软骨。发现肿瘤的其他部位包括假声带、真声带、会厌、声门下、梨状窦和环状软骨后区。64.9%的患者出现声音嘶哑。其他患者通常表现出与肿瘤的占位效应和位置相关的多种症状。所有患者均采用不同的技术和方法进行手术治疗。大多数患者存活且无残留疾病。目前有5例复发,无死亡病例。喉内神经鞘瘤可表现出多种症状。手术切除仍然是首选治疗方法,总体预后良好。

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