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鼻窦神经内分泌癌

Sino-nasal neuro-endocrine carcinoma.

作者信息

Chang Chia-Fan, Li Wing-Yin, Shu Chih-Hung, Ho Ching-Yin

机构信息

Department of Otolaryngology, Taipei Veterans General Hospital and National Yang Ming University, Taipei, Taiwan.

出版信息

Acta Otolaryngol. 2010 Mar;130(3):392-7. doi: 10.1080/00016480903148274.

Abstract

CONCLUSION

Patients with sino-nasal neuro-endocrine carcinoma should be managed by multi-modality treatment that includes surgery and postoperative chemo-radiotherapy as described in our treatment plan. Even though current combined therapy results in good disease control and survival rate, long-term follow-up is necessary.

OBJECTIVE

Neuro-endocrine carcinoma is an aggressive and rare malignant tumor of the sino-nasal tract, and its management remains divergent. The aim of this paper is to present our experience in the management of this kind of aggressive tumor and compare different treatment plans in order to draw up an effective strategy. Various treatment strategies were reviewed and assessed.

METHODS

Seven patients with biopsy-proven primary sino-nasal neuro-endocrine carcinoma from July 2004 to December 2006 were evaluated. The staging system was based on the American Joint Committee on Cancer Staging Manual of 2002. All of the patients underwent endoscopic or open surgery with curative intent. Six patients received postoperative chemo-radiotherapy.

RESULTS

The median follow-up after surgery was 43.5 months (range 26.9-57.7 months). One patient was T2N0M0, one was T3N0M0, four were T4aN0M0, and one was T4bN0M0. After endoscopic or open surgery and postoperative chemo-radiotherapy, six patients were alive with no evidence of recurrence. One patient had persistent tumor without clinical and imaging changes for 36.9 months. After the whole treatment course, one patient had sino-cutaneous fistula and underwent flap reconstruction. None had regional failure or distant metastasis during follow-up.

摘要

结论

鼻窦神经内分泌癌患者应采用多模式治疗,包括手术及术后放化疗,如我们的治疗方案所述。尽管目前的联合治疗能带来良好的疾病控制和生存率,但仍需长期随访。

目的

神经内分泌癌是鼻窦的一种侵袭性罕见恶性肿瘤,其治疗方法仍存在差异。本文旨在介绍我们在治疗这类侵袭性肿瘤方面的经验,并比较不同的治疗方案,以制定有效的策略。对各种治疗策略进行了回顾和评估。

方法

评估了2004年7月至2006年12月期间7例经活检证实为原发性鼻窦神经内分泌癌的患者。分期系统基于2002年美国癌症联合委员会分期手册。所有患者均接受了根治性的内镜或开放手术。6例患者接受了术后放化疗。

结果

术后中位随访时间为43.5个月(范围26.9 - 57.7个月)。1例为T2N0M0,1例为T3N0M0,4例为T4aN0M0,1例为T4bN0M0。在内镜或开放手术及术后放化疗后,6例患者存活且无复发迹象。1例患者肿瘤持续存在,临床和影像学无变化,持续36.9个月。整个治疗过程后,1例患者出现鼻皮肤瘘并接受了皮瓣重建。随访期间无一例出现区域复发或远处转移。

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