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双侧脑桥梗死中的非典型“九”综合征:一例报告

Atypical "nine" syndrome in bilateral pontine infarction: A case report.

作者信息

Cao Shugang, Wang Rongfeng, Xia Mingwu, Xu Wen'an

机构信息

Department of Neurology, Hefei Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.

出版信息

Medicine (Baltimore). 2019 Jul;98(28):e16378. doi: 10.1097/MD.0000000000016378.

Abstract

RATIONALE

"Nine" syndrome, that is "eight-and-a-half" syndrome associated with hemiplegia and hemidysesthesia, is a rare disorder. This study aimed to report a Chinese patient with acute bilateral pontine infarction manifesting as eight-and-a-half syndrome plus hemiplegia (atypical nine syndrome), and also the clinical and neuroimaging findings were explained and discussed with review of the literature.

PATIENT CONCERNS

A 79-year-old woman experienced sudden vertigo, nausea, vomiting, and weakness at her left arm and leg. The neurological examination disclosed her right horizontal gaze palsy, internuclear ophtalmoplegia (INO), and right-sided peripheral facial paralysis combined with slight left-sided hemiplegia, which were consistent with atypical nine syndrome.

DIAGNOSES

Cranial magnetic resonance imaging (MRI) displayed acute multiple ischemic infarction, involving bilateral pontine tegmentum, basilar part of right paramedian pontine, and left cerebellar hemisphere. Intracranial MR angiography (MRA) revealed right middle cerebral artery occlusion, no clear visualization of bilateral vertebral arteries, and basilar artery hypoplasia with stenotic segments.

INTERVENTIONS

Thrombolysis could not be performed due to the time window. The patient was given low molecular weight heparin for anticoagulation because of posterior circulation and progressive stroke.

OUTCOMES

The vertigo disappeared, and a notable improvement with minimal restriction in the right horizontal gaze and partial relief of her facial paralysis were found at discharge, while her left hemiparesis was fully resolved. No recurrence of cerebral infarction was observed during follow-up as well.

LESSONS

This case report with atypical nine syndrome is fairly rare. Nine syndrome may refer to the lesion located in unilateral tegmentum of the caudal pontine plus paramedian pontine, with an important localization value.

摘要

理论依据

“九”综合征,即伴有偏瘫和偏身感觉障碍的“八点五”综合征,是一种罕见的疾病。本研究旨在报告一名表现为八点五综合征加偏瘫(非典型九综合征)的急性双侧脑桥梗死的中国患者,并结合文献复习对其临床和神经影像学表现进行解释和讨论。

患者情况

一名79岁女性突发眩晕、恶心、呕吐,左侧手臂和腿部无力。神经系统检查发现其右侧水平凝视麻痹、核间性眼肌麻痹(INO)、右侧周围性面瘫合并轻度左侧偏瘫,符合非典型九综合征。

诊断

头颅磁共振成像(MRI)显示急性多发性缺血性梗死,累及双侧脑桥被盖、右侧脑桥旁正中基底部和左侧小脑半球。颅内磁共振血管造影(MRA)显示右侧大脑中动脉闭塞,双侧椎动脉显示不清,基底动脉发育不良并伴有狭窄段。

干预措施

由于时间窗问题无法进行溶栓治疗。因后循环及进展性卒中,给予患者低分子肝素抗凝。

结果

眩晕消失,出院时右侧水平凝视受限明显改善,面瘫部分缓解,左侧偏瘫完全恢复。随访期间未观察到脑梗死复发。

经验教训

本非典型九综合征病例报告相当罕见。九综合征可能提示病变位于脑桥尾端单侧被盖加旁正中脑桥,具有重要的定位价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c857/6641660/6fe6d4c8a0d5/medi-98-e16378-g001.jpg

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