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纯三叉神经运动神经病所致咀嚼肌局灶性萎缩:病例报告

Focal atrophy of the masticatory muscles caused by pure trigeminal motor neuropathy: case report.

作者信息

Wilson M H, Hodgson E J, Felstead A M

机构信息

Department of Oral and Maxillofacial Surgery, Royal United Hospital Bath NHS Trust, Combe Park, Bath BA1 3NG, United Kingdom.

Department of Oral and Maxillofacial Surgery, Royal United Hospital Bath NHS Trust, Combe Park, Bath BA1 3NG, United Kingdom.

出版信息

Br J Oral Maxillofac Surg. 2016 Jan;54(1):e13-4. doi: 10.1016/j.bjoms.2015.08.265. Epub 2015 Sep 18.

Abstract

Pure trigeminal motor neuropathy is rare and characterised by weakness of the mandibular motor branch with no signs of involvement of the trigeminal sensory or other cranial nerve. Its aetiology is unclear but it has been hypothesised that a viral infection may be a cause. Magnetic resonance imaging is useful in its diagnosis and typically shows loss of volume of the affected masticatory muscles and infiltration of fat. We describe the case of a 29-year-old woman who presented with a 12-year history of progressive facial asymmetry, which was later shown on imaging to be caused by unilateral atrophy of the masseter with compensatory contralateral hypertrophy.

摘要

纯三叉神经运动神经病较为罕见,其特征为下颌运动支无力,且无三叉神经感觉或其他颅神经受累迹象。其病因尚不清楚,但据推测病毒感染可能是一个原因。磁共振成像对其诊断有帮助,通常显示受累咀嚼肌体积减小及脂肪浸润。我们描述了一名29岁女性的病例,她有12年进行性面部不对称病史,影像学检查后来显示这是由咬肌单侧萎缩并伴有对侧代偿性肥大所致。

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