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腮腺内面神经鞘瘤:诊断与治疗的难题。

The intraparotid facial nerve schwannoma: a diagnostic and management conundrum.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Mayo Clinic School of Medicine, Rochester, MN 55905, USA.

出版信息

Am J Otolaryngol. 2012 Sep-Oct;33(5):497-504. doi: 10.1016/j.amjoto.2011.11.002. Epub 2011 Dec 19.

Abstract

OBJECTIVES

The aims of the study were (1) to review the management strategy and clinical outcomes of all intraparotid facial nerve (FN) schwannomas (PFNSs) treated at a single tertiary academic center from 1975 to 2010 and (2) to summarize all previously reported cases of PFNS in the international literature.

STUDY DESIGN

A retrospective cohort study and literature review.

METHODS

Fifteen patients were diagnosed and treated at the authors' institution from 1975 to 2010. In addition, 124 published cases were systematically reviewed.

RESULTS

The most common presentation of PFNS was a painless parotid mass with normal FN function. Eccentric, loosely attached intraparotid tumors underwent gross total resection with nerve preservation granting satisfactory postoperative FN function, whereas "inseparable" intraparotid tumors were observed in 8 cases with stable long-term size. Lesions that extended into the fallopian canal underwent complete resection with FN sacrifice and nerve grafting in 10 cases, whereas 1 patient received subtotal resection of the intraparotid portion with stereotactic radiotherapy targeting the intratemporal component.

CONCLUSIONS

Intraparotid FN schwannomas present similar to other primary salivary gland neoplasms, making an early diagnosis challenging. Intraoperative recognition of gross tumor characteristics and early histologic diagnosis with strategic biopsy are critical. Information including tumor location and extent, preoperative FN function, and the gross relationship between the tumor and the FN may guide the surgeon toward an optimal treatment plan emphasizing long-term neurologic preservation.

摘要

目的

本研究旨在(1)回顾 1975 年至 2010 年在一家三级学术中心治疗的所有腮腺内面神经(FN)神经鞘瘤(PFNS)的治疗策略和临床结果,以及(2)总结国际文献中所有以前报道的 PFNS 病例。

研究设计

回顾性队列研究和文献复习。

方法

1975 年至 2010 年,作者所在机构诊断并治疗了 15 例患者。此外,还对 124 例已发表的病例进行了系统回顾。

结果

PFNS 的最常见表现为无痛性腮腺肿块伴 FN 功能正常。偏心、松散附着的腮腺内肿瘤行大体全切除伴神经保留,术后 FN 功能满意,而 8 例“不可分离”的腮腺内肿瘤则观察到长期稳定的大小。病变延伸至输卵管者行 FN 牺牲和神经移植的完全切除,10 例患者行全切除,1 例患者行腮腺内部分切除,同时对颞内部分进行立体定向放疗。

结论

腮腺内 FN 神经鞘瘤与其他原发性涎腺肿瘤表现相似,早期诊断具有挑战性。术中识别大体肿瘤特征和早期组织学诊断,以及有针对性的活检至关重要。包括肿瘤位置和范围、术前 FN 功能以及肿瘤与 FN 之间的大体关系等信息,可能有助于外科医生制定最佳治疗计划,强调长期神经保护。

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