嗅神经母细胞瘤的内镜切除术。

Endoscopic resection of esthesioneuroblastoma.

作者信息

Casiano R R, Numa W A, Falquez A M

机构信息

Department of Otolaryngology, University of Miami School of Medicine, Florida 33101, USA.

出版信息

Am J Rhinol. 2001 Jul-Aug;15(4):271-9.

DOI:
Abstract

Esthesioneuroblastoma (olfactory neuroblastoma) is a rare malignant neoplasm originating from neuroepithelial cells. Treatment for this tumor has traditionally required a craniofacial resection through an external approach. The safety and efficacy of transnasal endoscopic resection is uknown. A series of five patients with Kadish stage A or B lesions of the anterior skull base were resected and immediately reconstructed endoscopically over a nine-year period. There were 2 males and 3 females with a mean age of 64 years. Three patients were treated primarily and two were treated secondarily for recurrences after failing a traditional external craniofacial resection and postoperative radiotherapy. All primary lesions received adjuvant radiotherapy. The mean follow-up time was 31 months. All patients were discharged within 4 days or less. Operative complications included temporary postoperative infraorbital anesthesia (1 patient), unplanned cerebrospinal fluid leak (1 patient), and can orbital hematoma (1 patient). None of these complications resulted in any permanent sequelae. Two patients had prolonged nasal crusting for up to one year due to a variety of factors; large cavities, radiation therapy, and exposed lyophilized dural graft. However, all skull base defects healed without any short- or long-term sequelae. There have been no local recurrences. Two patients (1 primary and 1 secondary) developed regional metastasis to the orbit or cervical lymph nodes managed with primary transorbital excision or modified neck dissection, respectively. All but one patient remain free of disease by clinical, endoscopic, and radiographic (CT or MRI) surveillance. The remaining patient recurred distally as an undifferentiated carcinoma in his temporal bone and lungs 12 months after the initial resection. In experienced hands select cases of esthesioneuroblastoma can be safely excised and reconstructed endoscopically with comparable degrees of tissue removal as with external approaches. Short-term oncologic results in this mall series of patients appear to be comparable to traditional methods. Longer follow-up on a larger series of patients is warranted.

摘要

嗅神经母细胞瘤(嗅觉神经母细胞瘤)是一种起源于神经上皮细胞的罕见恶性肿瘤。传统上,该肿瘤的治疗需要通过外部入路进行颅面切除术。经鼻内镜切除术的安全性和有效性尚不清楚。在九年的时间里,对一系列五例卡迪什分期为A或B期的前颅底病变患者进行了切除,并立即在内镜下进行了重建。其中男性2例,女性3例,平均年龄64岁。3例患者为初次治疗,2例患者在传统的外部颅面切除术和术后放疗失败后复发,进行二次治疗。所有原发性病变均接受辅助放疗。平均随访时间为31个月。所有患者均在4天或更短时间内出院。手术并发症包括术后暂时性眶下麻醉(1例)、意外脑脊液漏(1例)和眶周血肿(1例)。这些并发症均未导致任何永久性后遗症。2例患者由于多种因素,包括大腔隙、放疗和暴露的冻干硬脑膜移植物,出现长达一年的长期鼻痂。然而,所有颅底缺损均愈合,无任何短期或长期后遗症。无局部复发。2例患者(1例原发性和1例继发性)分别出现眼眶或颈部淋巴结区域转移,分别采用原发性经眶切除术或改良颈部清扫术进行处理。除1例患者外,所有患者通过临床、内镜和影像学(CT或MRI)监测均无疾病复发。其余1例患者在初次切除术后12个月,在颞骨和肺部远端复发为未分化癌。在经验丰富的医生手中,对于某些嗅神经母细胞瘤病例,可以安全地在内镜下切除并重建,组织切除程度与外部入路相当。这一小系列患者的短期肿瘤学结果似乎与传统方法相当。需要对更多患者进行更长时间的随访。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索