感觉神经母细胞瘤(嗅觉神经母细胞瘤):手术入路和颅底切除的概述和范围。

IF 0.6 Q4 CLINICAL NEUROLOGY
Journal of Neurological Surgery Reports Pub Date : 2022-07-10 eCollection Date: 2022-07-01 DOI:10.1055/s-0042-1753519
Emily E Karp, Jamie J Van Gompel, Garret Choby
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引用次数: 3

摘要

摘要感觉神经母细胞瘤是一种罕见的源自嗅觉上皮的恶性肿瘤。治疗以手术切除为主,对晚期卡迪什病和Hyams分级高的患者优先考虑辅助治疗。在现代,与许多其他鼻窦恶性肿瘤相比,感觉神经母细胞瘤的总体结果是有利的,5年总生存率估计为80%。在选择最佳手术入路时,外科医生必须考虑能切除负缘和充分重建的入路。在适当选择的患者中,内镜结果至少与开放入路相当,单侧内镜入路可用于选择嗅觉保留病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Esthesioneuroblastoma (Olfactory Neuroblastoma): Overview and Extent of Surgical Approach and Skull Base Resection.

Esthesioneuroblastoma (Olfactory Neuroblastoma): Overview and Extent of Surgical Approach and Skull Base Resection.

Esthesioneuroblastoma (Olfactory Neuroblastoma): Overview and Extent of Surgical Approach and Skull Base Resection.

Esthesioneuroblastoma is a rare malignancy originating from the olfactory epithelium. Treatment consists of surgical resection with strong consideration for adjuvant treatment in advanced Kadish stage and high Hyams grade. In the modern era, overall outcomes for esthesioneuroblastoma are favorable compared with many other sinonasal malignancies with 5-year overall survival estimated to be 80%. When selecting the optimal surgical approach, the surgeon must consider the approach that will allow for a negative margin resection and adequate reconstruction. In appropriately selected patients, endoscopic outcomes appear at least equivalent to open approaches and unilateral endoscopic approach may be used in select olfactory preservation cases.

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