三叉神经鞘瘤

Breno Nery, Marcelo Nery Silva, Rodrigo Antônio Fernandes Costa, Leandro César Tângari Pereira, Eduardo Quaggio, Fred Bernardes Filho, George Peter Stevens
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引用次数: 0

摘要

三叉神经鞘瘤(TS)是发生在三叉神经各个部位的罕见疾病,发病率在40岁至50岁之间达到高峰,在女性中更为常见。患者通常表现为三叉神经功能障碍。根据肿瘤的地形,可以使用不同的方法来获得肿瘤的总切除。三叉神经鞘瘤的分类,方法的细微差别,病理,术后护理和结果修订如下。总之,在处理这类病变时,解剖学知识和对疾病的理解是必不可少的,尽管它们很少见,但我们必须坚持手术技术,并致力于患者的术后功能结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trigeminal Schwannomas
Trigeminal schwannomas (TS) are rare entities occurring in various trigeminal nerve locations and present a peak incidence between the fourth and fifth decades of life, being more common in women. Patients usually present with symptoms of trigeminal nerve dysfunction. Depending on the tumor’s topography, various approaches might be used to obtain its gross total resection. Trigeminal schwannoma’s classification, nuances of the approaches, pathology, postoperative care, and outcomes are revised as follows. In conclusion, anatomical knowledge and the disease’s comprehension are essential when dealing with such lesions, and despite their rarity, we must be obstinately committed to the surgical technique and devoted to the patient’s functional postoperative outcome.
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