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[鳃盖综合征:两例报告及文献综述]

[Biopercular syndrome: report of two cases and literature review].

作者信息

Millán Paula Andrea, Montes María Isabel, Uribe Carlos Santiago, Cabrera Dagoberto, Arboleda Alejandra

机构信息

Sección de Neurología Clínica, Hospital Universitario San Vicente de Paúl, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.

出版信息

Biomedica. 2008 Jun;28(2):183-90.

Abstract

The anterior opercular or biopercular syndrome is a cortical pseudobulbar palsy due to bilateral lesions of the anterior brain operculum. It is characterized by preservation of reflex function and automatic activity, without mental impairment. Two cases are reported herein and the relevant literature reviewed. The first case was a 73-year-old female with a history of a stroke occurring seven years previously, without sequelae in the interim. She presented with sudden loss of consciousness. The neurological examination showed a right facial central palsy and anarthria, with reflex acts such as smiling, blinking and yawning, not elicited by commands; she also had a right hemiparesis and walking impairment. A brain CT scan showed an old ischemic infarction in the region of the right medial cerebral artery. Because the right motor involvement did not correlate with the findings of the initial CT scan, another CT scan two days later showed an acute brain infarction in the vicinity of the left medial cerebral artery. The second case was an 8-year-old girl with mental retardation and impairment of verbal development, caused by of biopercular pachygyria. Facio-pharyngo-glosso-masticatory diplegia and volitional selective palsy of the oro-facial muscles was seen in both patients. The neuropsychological assessment showed cognitive, emotional and social interaction impairment in both cases -as part of the frontal convexity syndrome in the first case and of mental retardation in the second. The two patients had difficulty in mastication and swallowing. The prognosis for recovery of verbal capacity is poor, although generally most patients recover the ability to swallow.

摘要

前岛盖或双侧岛盖综合征是一种由于双侧大脑前岛盖病变引起的皮质假性延髓麻痹。其特征是反射功能和自动活动保留,无智力损害。本文报告2例并复习相关文献。首例为73岁女性,有7年前卒中史,在此期间无后遗症。她突发意识丧失。神经系统检查显示右侧中枢性面瘫和构音障碍,微笑、眨眼和打哈欠等反射动作不能被指令诱发;她还有右侧偏瘫和行走障碍。脑部CT扫描显示右侧大脑中动脉区域有陈旧性缺血性梗死。由于右侧运动受累与初次CT扫描结果不符,两天后另一次CT扫描显示左侧大脑中动脉附近有急性脑梗死。第二例是一名8岁女孩,因双侧岛盖巨脑回导致智力发育迟缓及语言发育障碍。两名患者均出现面-咽-舌-咀嚼肌双侧瘫痪及口面部肌肉的随意选择性麻痹。神经心理学评估显示两例均有认知、情感和社会交往障碍——首例为额叶凸面综合征的一部分,第二例为智力发育迟缓的一部分。两名患者咀嚼和吞咽困难。虽然一般大多数患者能恢复吞咽能力,但语言能力恢复的预后较差。

相似文献

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[Biopercular lesion with inverse dissociation].
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Anterior biopercular syndrome caused by unilateral infarction.
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