首页> 美国卫生研究院文献>Case Reports in Neurology >Millard-Gubler Syndrome Associated with Cerebellar Ataxia in a Patient with Isolated Paramedian Pontine Infarction − A Rarely Observed Combination with a Benign Prognosis: A Case Report
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Millard-Gubler Syndrome Associated with Cerebellar Ataxia in a Patient with Isolated Paramedian Pontine Infarction − A Rarely Observed Combination with a Benign Prognosis: A Case Report

机译:Millard-Gubler综合征与小脑共济失调相关的患者患者与隔离的副护理症患者梗死 - 很少观察到与良性预后的组合:案例报告

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摘要

Isolated pontine infarction accounts for 7% of all ischemic strokes. Millard-Gubler syndrome is a clinical syndrome which occurs following lesions involving the ventral portion of the caudal pons, resulting in classic clinical features such as ipsilateral abducens and facial nerve palsy and contralateral hemiparesis. We report the case of a 55-year-old male patient having presented to the Yehuleshet Specialty Clinic 6 years back with sudden-onset dysarthria and appendicular ataxia of 10 days duration. He reported having right hemibody weakness and blurred vision, which have significantly improved since then. He had a history of smoking of 30 pack-years. However, he quit smoking 8 years ago. There was no history of prior stroke, transient ischemic attack, diabetes, hypertension, head trauma, or dyslipidemia. On examination, he had horizontal left gaze palsy with horizontal nystagmus suggesting left-sided 6th cranial nerve palsy. He had mild left-sided facial palsy causing dysarthric speech. Right upper limb dysmetria was observed during examination; otherwise, motor, sensory, fundus, and gait examination results were normal. He had low serum vitamin D. Brain magnetic resonance imaging examination showed a 25 × 10 mm segmental lesion in the left median pons involving the basis pontis and tegmentum section. The lesion had T2 and T1 abnormal prolongation with no diffusion restriction, suggesting a subacute pontine infarct. The patient was managed with aspirin 325 mg, atorvastatin 80 mg, physical therapy, and vitamin D supplementation, and advised on behavioral risk factors. Six years after his isolated pontine infarction, the patient is fully recovered from dysarthria, facial palsy, hemiparesis, right-sided appendicular ataxia, and horizontal nystagmus, and the follow-up brain MRI showed radiological evidence of chronic paramedian pontine perforator infarction. Millard-Gubler syndrome may present with cerebellar ataxia if the paramedian pontine infarction area slightly extends laterally, affecting the middle cerebellar peduncles. Isolated pontine infarction may have a good prognosis if diagnosed and managed early.
机译:孤立的粪便梗死占所有缺血卒中的7%。 Millard-Gubler综合征是一种临床综合征,其发生涉及尾巴腹侧部分的病变之后,导致诸如同侧Abducens和面部神经麻痹和对侧血管的经典临床特征。我们举报了55岁的男性患者在6年后举行了55岁的男性患者,突然发作了讨厌的讨厌和10天持续时间的阑尾症。他报告过正确的血腥弱点和模糊的视力,从那时起就显着提高了。他有30次吸烟的历史。然而,他在8年前戒烟了。没有先前中风,短暂性缺血性发作,糖尿病,高血压,头部创伤或血脂血症的历史。在考试时,他用水平的乳腺左凝视麻痹,横向的第6次颅神经麻痹。他患有轻度左侧面部麻痹,导致发狂的言论。在检查期间观察到右上肢渗滤菌;否则,电机,感官,眼底和步态检查结果正常。他的血清维生素D.脑磁共振成像检查脑磁共振成像检查显示为涉及基础Pontis和Tegmentum部分的左级中位数的25×10mm节段性病变。病变具有T2和T1异常延长,没有扩散限制,表明亚急性粪便梗塞。患者用阿司匹林325毫克,阿草醛胺80毫克,物理治疗和维生素D补充,并建议行为危险因素。六年后患者患者梗死后,患者完全从扰乱,面部麻痹,血管血管术中恢复,右侧垂直的垂直共济失调和水平眼动脉瘤,随访脑MRI显示出慢性主管粪便穿孔梗死的放射性证据。米尔德 - Gubler综合征可能存在小脑共济失调,如果Paramedian Pontine梗死区域横向侧向横向延伸,影响中间人的章节。如果早期诊断和管理,孤立的粪便梗死可能具有良好的预后。

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