Suppr超能文献

颈交感神经链神经鞘瘤

Cervical sympathetic chain schwannoma.

作者信息

Wax Mark K, Shiley Samuel G, Robinson Jamie L, Weissman Jane L

机构信息

Department of Otolaryngology/Head and Neck Surgery, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, U.S.A.

出版信息

Laryngoscope. 2004 Dec;114(12):2210-3. doi: 10.1097/01.mlg.0000149460.98629.42.

Abstract

OBJECTIVES

Schwannomas are benign, slow-growing tumors that arise from nerves. Those originating from the sympathetic cervical chain are rare. We describe our experience with the clinical presentation, surgical management, and outcomes of patients with this pathology.

STUDY DESIGN

Retrospective chart review of a case series in a tertiary referral center.

METHODS

Four cases of cervical sympathetic chain schwannomas were reviewed. Patients presented with either an asymptomatic neck mass discovered on routine physical examination (1 patient), an enlarging neck mass (2), or an acute onset of a Horner's syndrome (1). All patients underwent preoperative imaging (magnetic resonance imaging, computed tomography, or both).

RESULTS

The location and soft-tissue characteristics of the mass, along with displacement of the carotid sheath vessels, were typical of a cervical sympathetic chain schwannoma. All patients underwent surgical excision of the mass. Postoperative Horner's syndrome was encountered in all patients. First bite syndrome was encountered in two patients.

CONCLUSIONS

Cervical sympathetic chain schwannomas are rare tumors. Preoperative imaging characteristics facilitate the diagnosis. First bite syndrome can occur and may be debilitating postoperatively. Long-term prognosis is excellent.

摘要

目的

施万细胞瘤是起源于神经的良性、生长缓慢的肿瘤。起源于颈交感神经链的施万细胞瘤较为罕见。我们描述了我们对患有这种病理情况的患者的临床表现、手术治疗及结果的经验。

研究设计

对一家三级转诊中心的病例系列进行回顾性病历审查。

方法

回顾了4例颈交感神经链施万细胞瘤病例。患者表现为在常规体格检查中发现的无症状颈部肿块(1例患者)、逐渐增大的颈部肿块(2例)或霍纳综合征急性发作(1例)。所有患者均接受了术前影像学检查(磁共振成像、计算机断层扫描或两者均有)。

结果

肿块的位置和软组织特征,以及颈动脉鞘血管的移位,是颈交感神经链施万细胞瘤的典型表现。所有患者均接受了肿块的手术切除。所有患者术后均出现霍纳综合征。2例患者出现了初咬综合征。

结论

颈交感神经链施万细胞瘤是罕见肿瘤。术前影像学特征有助于诊断。初咬综合征可能发生,且术后可能使人衰弱。长期预后良好。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验