1 Department of Otorhinolaryngology-Head and Neck Surgery, IRCCS San Raffaele Hospital, Vita-Salute University, Milan, Italy.
2 Department of Pathology, IRCCS San Raffaele Vita-Salute University, Milan, Italy.
Otolaryngol Head Neck Surg. 2018 Feb;158(2):222-231. doi: 10.1177/0194599817735508. Epub 2017 Oct 17.
Objective This review summarizes the clinical features, diagnostic workup, and surgical treatment of laryngeal schwannoma with the aim of providing guidance for the management of this rare disease. The collated data allowed the statistical testing of several hypotheses, including the efficacy of endoscopic vs open surgical intervention and the usefulness of preoperative biopsy. Data Sources PubMed, Google Scholar, Cochrane, and SCOPUS. Review Methods Basic epidemiological and clinical presentation data were collated together with details of diagnostic image modality, lesion attributes, and the use of preoperative biopsy. Surgical approach to intervention and outcome was also collated and simple statistical analyses applied. Results The 60 original articles selected provided a combined cohort of 74 patients for review. The combined data revealed that schwannoma with pedunculated morphology were always safely removed by endoscopic resection regardless of size and should be treated as a separate entity. Of the nonpedunculated schwannoma, larger tumors were more likely to undergo an open approach, which in turn was associated with higher rates of tracheotomy and postoperative vocal fold paralysis. The small cohort did not reveal a significant association between surgery type and persistent disease. Interestingly, the data revealed a significant association between the use of incisional biopsy and persistent disease. Cases exhibiting extralaryngeal extension of the lesion were shown to exclusively belong to patients with neurofibromatosis/schwannomatosis syndromes. Conclusions Taken together, these findings suggest that incisional biopsy should be avoided, and given the benign nature of the pathology, the least invasive radical approach should be employed.
本文综述了喉神经鞘瘤的临床特征、诊断方法和手术治疗,旨在为这种罕见疾病的治疗提供指导。所收集的数据允许对几个假设进行统计检验,包括内镜与开放手术干预的疗效,以及术前活检的有用性。
PubMed、Google Scholar、Cochrane 和 SCOPUS。
收集了基本的流行病学和临床表现数据,以及诊断影像学模式、病变特征和术前活检的详细信息。还收集了手术干预和结果,并进行了简单的统计分析。
选择的 60 篇原始文章提供了 74 例患者的综合队列进行回顾。综合数据表明,带蒂形态的神经鞘瘤无论大小,均可通过内镜切除安全切除,应视为单独的实体。对于无蒂神经鞘瘤,较大的肿瘤更有可能采用开放手术,这反过来又与气管切开术和术后声带麻痹的发生率较高相关。小队列并未显示手术类型与持续性疾病之间存在显著关联。有趣的是,数据显示,手术类型与持续性疾病之间存在显著关联。表现为声带外扩展的病变病例仅见于神经纤维瘤病/神经鞘瘤病综合征患者。
综上所述,这些发现表明应避免使用切开活检,鉴于该病变的良性性质,应采用最微创的根治性方法。