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伴有颈内动脉夹层的亚急性舌下神经麻痹

Subacute hypoglossal nerve paresis with internal carotid artery dissection.

作者信息

Lindsay Fred W, Mullin David, Keefe Michael A

机构信息

Department of Otolaryngology-Head and Neck Surgery, Naval Medical Center, San Diego, CA 92134, USA.

出版信息

Laryngoscope. 2003 Sep;113(9):1530-3. doi: 10.1097/00005537-200309000-00022.

Abstract

OBJECTIVES

To describe a case of an isolated hypoglossal nerve palsy in a patient with a spontaneous internal carotid artery dissection (ICAD). This condition is a well-recognized cause of cerebral ischemic stroke in patients younger than 45 years of age. Isolated cranial nerve neuropathy is a rare presentation. More common manifestations include incomplete hemiparesis, hemicrania, Horner syndrome, cervical bruit, pulsatile tinnitus, and multiple cranial nerve palsies.

METHODS

A comprehensive literature search (Ovid, MEDLINE) for the presentation, diagnostic evaluation, treatment, and outcome of patients with internal carotid artery dissection was performed.

RESULTS

A 43-year-old man presented with a 3-week history of mild dysarthria. There was no history of craniocervical trauma. The physical examination revealed an isolated left hypoglossal nerve paresis. Magnetic resonance imaging and angiography findings were consistent with a left skull base ICAD. The patient was successfully treated with anticoagulation therapy. The current rate of cranial nerve involvement is estimated at 10% of all ICADs. This is the second report of isolated hypoglossal nerve palsy without hemicrania in a case of atraumatic ICAD.

CONCLUSIONS

Patients with an ICAD infrequently present to the otolaryngologist because of its head and neck manifestations. It is crucial to recognize atypical findings and to perform an accurate and prompt diagnostic evaluation. The foundation of treatment is aggressive anticoagulation, with surgical or radiologic intervention reserved for cases demonstrating life-threatening progression.

摘要

目的

描述一例自发性颈内动脉夹层(ICAD)患者出现孤立性舌下神经麻痹的病例。这种情况是45岁以下患者脑缺血性卒中的一个公认病因。孤立性颅神经神经病变是一种罕见的表现。更常见的表现包括不完全偏瘫、偏头痛、霍纳综合征、颈部杂音、搏动性耳鸣和多发性颅神经麻痹。

方法

对颈内动脉夹层患者的临床表现、诊断评估、治疗及预后进行全面的文献检索(Ovid,MEDLINE)。

结果

一名43岁男性,有3周轻度构音障碍病史。无颅颈外伤史。体格检查发现孤立性左侧舌下神经麻痹。磁共振成像和血管造影结果与左侧颅底ICAD一致。该患者接受抗凝治疗后成功治愈。目前估计颅神经受累发生率在所有ICAD中占10%。这是第二例无偏头痛的孤立性舌下神经麻痹伴非创伤性ICAD的报告。

结论

由于ICAD的头颈部表现,此类患者很少就诊于耳鼻喉科医生。认识非典型表现并进行准确及时的诊断评估至关重要。治疗的基础是积极抗凝,对于显示有危及生命进展的病例可采用手术或放射介入治疗。

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