Suppr超能文献

[一名无2型神经纤维瘤病遗传或临床特征患者的双侧耳蜗内神经鞘瘤。德文版]

[Bilateral intracochlear schwannomas in a patient with no genetic or clinical features of neurofibromatosis type 2. German version].

作者信息

Withers S, Plontke S K, Boeddinghaus R, Kuthubutheen J, Atlas M

机构信息

Ear Science Institute of Australia, School of Surgery, University of Western Australia, 1/1 Salvado Road, 6008, Subiaco, Australien.

Universitätsklinik und Poliklinik für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Deutschland.

出版信息

HNO. 2020 Jul;68(7):534-538. doi: 10.1007/s00106-019-00751-w.

Abstract

Schwannomas of the eighth cranial nerve are benign tumours commonly found in the internal auditory meatus or in the cerebellopontine angle. In most cases, they arise from the inferior or vestibular portion of the vestibular nerve. Rarely, these tumours present in the inner ear and are then called intralabyrinthine schwannomas. Bilateral schwannomas are known in neurofibromatosis type 2 (NF2). Bilateral and ipsilateral, multilocular sporadic schwannomas of the eighth cranial nerve have been described as extremely rare findings. This report describes the first case of bilateral sporadic intracochlear schwannomas in a patient with no genetic or clinical features of NF2.

摘要

第八颅神经鞘瘤是常见于内耳道或桥小脑角的良性肿瘤。在大多数情况下,它们起源于前庭神经的下部或前庭部分。很少有这些肿瘤出现在内耳,此时被称为迷路内神经鞘瘤。双侧神经鞘瘤见于2型神经纤维瘤病(NF2)。双侧和同侧的第八颅神经多房性散发性神经鞘瘤被描述为极其罕见的发现。本报告描述了首例无NF2遗传或临床特征患者的双侧散发性耳蜗内神经鞘瘤。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验