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耳蜗内神经鞘瘤:诊断与治疗

Intracochlear schwannoma: diagnosis and management.

作者信息

Bittencourt Aline Gomes, Alves Ricardo Dourado, Ikari Liliane Satomi, Burke Patrick Rademaker, Gebrim Eloisa Maria Santiago, Bento Ricardo Ferreira

机构信息

Department of Otolaryngology, Universidade de São Paulo, São Paulo, São Paulo, Brazil.

Department of Radiology, Universidade de São Paulo, São Paulo, São Paulo, Brazil.

出版信息

Int Arch Otorhinolaryngol. 2014 Jul;18(3):322-4. doi: 10.1055/s-0033-1364170. Epub 2014 Jan 7.

DOI:10.1055/s-0033-1364170
PMID:25992114
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4296998/
Abstract

Introduction Schwannomas of the eighth cranial nerve are benign tumors that usually occur in the internal auditory canal or the cerebellopontine angle cistern. Rarely, these tumors may originate from the neural elements within the vestibule, cochlea, or semicircular canals and are called intralabyrinthine schwannomas. Intracochlear schwannomas (ICSs) represent a small percentage of these tumors, and their diagnosis is based on high-resolution magnetic resonance imaging (MRI). Objectives To report the clinical and radiologic features and audiometric testing results of an ICS in a 48-year-old man after a 22-month follow-up period. Resumed Report A patient with an 8-year history of persistent tinnitus in his right ear, combined with ipsilateral progressive hearing loss and aural fullness. Audiometry revealed normal hearing in the left ear and a moderate to severe sensorineural hearing loss in the right ear, with decreased speech reception threshold and word recognition score, compared with the exam performed 5 years previously. MRI showed a small intracochlear nodular lesion in the modiolus, isointense on T1 with a high contrast enhancement on T1 postgadolinium images. During the follow-up period, there were no radiologic changes on imaging studies. Thus, a wait-and-scan policy was chosen as the lesion remained stable with no considerable growth and the patient still presents with residual hearing. Conclusions Once diagnosed, not all ICS patients require surgery. Treatment options for ICS include stereotactic radiotherapy and rescanning policy, depending on the tumor's size, evidence of the tumor's growth, degree of hearing loss, intractable vestibular symptoms, concern about the pathologic diagnosis, and the patient's other medical conditions.

摘要

引言

第八颅神经鞘瘤是一种良性肿瘤,通常发生在内耳道或桥小脑角池。这些肿瘤很少起源于前庭、耳蜗或半规管内的神经成分,被称为迷路内神经鞘瘤。耳蜗内神经鞘瘤(ICSs)在这些肿瘤中占比很小,其诊断基于高分辨率磁共振成像(MRI)。目的:报告一名48岁男性ICS患者在22个月随访期后的临床、放射学特征及听力测试结果。病例报告:一名患者有8年的右耳持续性耳鸣病史,伴有同侧进行性听力损失和耳闷。听力测试显示左耳听力正常,右耳中度至重度感音神经性听力损失,与5年前的检查相比,言语接受阈值和单词识别分数降低。MRI显示蜗轴内有一个小的耳蜗内结节性病变,T1加权像上等信号,T1加权像钆增强后呈高对比度增强。在随访期间,影像学检查未见放射学变化。因此,选择了等待观察策略,因为病变保持稳定,没有明显生长,且患者仍有残余听力。结论:一旦确诊,并非所有ICS患者都需要手术。ICS的治疗选择包括立体定向放射治疗和再次扫描策略,这取决于肿瘤的大小、肿瘤生长的证据、听力损失程度、顽固性前庭症状、对病理诊断的担忧以及患者的其他医疗状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/dab74a249ed2/10-1055-s-0033-1364170-i0051cr-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/cab9f8ddf7f2/10-1055-s-0033-1364170-i0051cr-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/d7f0aff3f9df/10-1055-s-0033-1364170-i0051cr-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/dab74a249ed2/10-1055-s-0033-1364170-i0051cr-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/cab9f8ddf7f2/10-1055-s-0033-1364170-i0051cr-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/d7f0aff3f9df/10-1055-s-0033-1364170-i0051cr-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe4/4296998/dab74a249ed2/10-1055-s-0033-1364170-i0051cr-3.jpg

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