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鼻窦黏膜黑色素瘤:一项44例病例研究及文献分析。

Sinonasal mucosal melanoma: A 44-case study and literature analysis.

作者信息

Dréno M, Georges M, Espitalier F, Ferron C, Charnolé A, Dréno B, Malard O

机构信息

Service d'ORL et de Chirurgie Cervico-Faciale, Centre Hospitalier Universitaire, 1 Place Alexis-Ricordeau, 44093 Nantes Cedex 1, France.

Service d'Anatomopathologie, Centre Hospitalier Universitaire, 1 Place Alexis-Ricordeau, 44093 Nantes Cedex 1, France.

出版信息

Eur Ann Otorhinolaryngol Head Neck Dis. 2017 Sep;134(4):237-242. doi: 10.1016/j.anorl.2017.02.003. Epub 2017 Apr 22.

DOI:10.1016/j.anorl.2017.02.003
PMID:28442409
Abstract

OBJECTIVES

Sinonasal mucosal melanoma is a rare disease, representing 4% of nasal cavity and paranasal sinus malignancies. The aim of this study was to assess the clinical characteristics, progression and treatment of this disease and to identify prognostic factors.

MATERIAL AND METHODS

This retrospective review presents a cohort of 44 patients treated for a melanoma arising from the nasal cavity and paranasal sinuses, in the ENT Head and Neck Surgery Department of the University Hospital of Nantes (France) between 1988 and 2015.

RESULTS

Mean age at diagnosis was 71.2 years. The main signs at diagnosis were epistaxis and unilateral nasal obstruction. 25% of patients were initially classified as T4. Surgical treatment was performed in 42 patients. Postoperative radiotherapy was performed in 19 cases and adjuvant immunotherapy in 14 cases. Mean follow-up was 50 months. Cumulative overall survival was 71.5% at 1 year and 33% at 5 years. Clinically, headache, facial pain and trigeminal V2 nerve anesthesia were significant factors for poor prognosis. Exclusively nasal involvement was a factor for better overall survival than sinus involvement. Adjuvant radiation therapy showed a non-significant trend toward improved local control.

CONCLUSIONS

Mucosal melanoma of the sinonasal cavities has poor prognosis due to high metastatic potential. Surgical resection followed by radiation therapy is the main treatment. There is no consensus regarding new systemic adjuvant treatments in this indication, unlike for primary cutaneous melanoma.

摘要

目的

鼻窦黏膜黑色素瘤是一种罕见疾病,占鼻腔和鼻窦恶性肿瘤的4%。本研究的目的是评估该疾病的临床特征、进展和治疗情况,并确定预后因素。

材料与方法

本回顾性研究纳入了1988年至2015年间在法国南特大学医院耳鼻喉头颈外科接受治疗的44例鼻腔和鼻窦黑色素瘤患者。

结果

诊断时的平均年龄为71.2岁。诊断时的主要症状是鼻出血和单侧鼻塞。25%的患者最初被归类为T4期。42例患者接受了手术治疗。19例患者术后接受了放疗,14例患者接受了辅助免疫治疗。平均随访时间为50个月。1年时的累积总生存率为71.5%,5年时为33%。临床上,头痛、面部疼痛和三叉神经V2支麻醉是预后不良的重要因素。仅累及鼻腔是总体生存率优于累及鼻窦的一个因素。辅助放疗在改善局部控制方面显示出不显著的趋势。

结论

由于转移潜力高,鼻窦黏膜黑色素瘤预后较差。手术切除后放疗是主要治疗方法。与原发性皮肤黑色素瘤不同,对于这种适应症的新的全身辅助治疗尚无共识。

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