Shibata Akio, Kimura Masashi, Ishibashi Kenichiro, Umemura Masahiro
Clinical Fellow, Department of Oral and Maxillofacial Surgery, Ogaki Municipal Hospital, Ogaki, Japan.
Clinical Fellow, Department of Oral and Maxillofacial Surgery, Ogaki Municipal Hospital, Ogaki, Japan.
J Oral Maxillofac Surg. 2018 Jul;76(7):1454-1459. doi: 10.1016/j.joms.2018.01.019. Epub 2018 Feb 2.
Hypoglossal nerve palsy (HNP) is a common finding in neurologic diseases when associated with other cranial nerve palsies or further pathology and exhibits characteristic clinical manifestations, including unilateral atrophy of the musculature of the tongue. It occasionally appears as the initial or solitary sign of an intracranial or extracranial space-occupying lesion, head or neck injury, or vascular abnormality of the internal carotid artery. There are few cases of idiopathic isolated unilateral HNP, which should be diagnosed through exclusion. This report describes 2 patients who had different outcomes and presents a literature review of idiopathic isolated unilateral HNP. Case 1 was a 71-year-old man who was referred with a 1-month history of dysphagia and speech impairment. Intraoral examination disclosed marked left-side hemiatrophy of the tongue and deviation toward the left on protrusion. At coronal Tl-weighted magnetic resonance imaging, left-side hemiatrophy of the tongue was clearly visible through deviation of the median septum to the left. The patient was diagnosed with idiopathic isolated unilateral HNP through exclusion and was treated with steroids and mecobalamin, but he did not recover. Case 2 was a 32-year-old man complaining of tongue weakness for 2 days. On examination, left HNP was evident, with deviation of the tongue to the left on protrusion. He was diagnosed with idiopathic isolated unilateral HNP through exclusion and was treated with steroids. After 3 weeks, the patient had completely recovered. To the best of the authors' knowledge, this is the first detailed literature review on idiopathic isolated unilateral HNP. This condition is very rare but should be considered for diagnosis. It warrants a thorough and stepwise approach for etiologic diagnosis.
舌下神经麻痹(HNP)在神经系统疾病中较为常见,常与其他颅神经麻痹或进一步的病变相关,并表现出特征性的临床表现,包括舌肌单侧萎缩。它偶尔作为颅内或颅外占位性病变、头部或颈部损伤或颈内动脉血管异常的初始或唯一症状出现。特发性孤立性单侧HNP病例较少,应通过排除法进行诊断。本报告描述了2例结局不同的患者,并对特发性孤立性单侧HNP进行了文献综述。病例1是一名71岁男性,因吞咽困难和言语障碍1个月前来就诊。口腔检查发现舌左侧明显半侧萎缩,伸出时偏向左侧。在冠状位T1加权磁共振成像上,通过正中隔向左偏移可清晰看到舌左侧半侧萎缩。该患者经排除诊断为特发性孤立性单侧HNP,接受了类固醇和甲钴胺治疗,但未恢复。病例2是一名32岁男性,主诉舌肌无力2天。检查时,左侧HNP明显,伸出时舌偏向左侧。他经排除诊断为特发性孤立性单侧HNP,并接受了类固醇治疗。3周后,患者完全康复。据作者所知,这是关于特发性孤立性单侧HNP的首次详细文献综述。这种情况非常罕见,但在诊断时应予以考虑。病因诊断需要采取全面且逐步的方法。