孤立性双侧脑梗表现假性球麻痹和四肢瘫1例。

Namwoo Kwon, Woo In Choi, Hyoung Seop Kim
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摘要

双侧脑梗是脑卒中患者中一种非常罕见的疾病。先前报道的BCPI病例报告的主要临床表现与闭锁综合征或持续植物人状态有关。在此,我们报告一位患有假性球麻痹和四肢瘫痪的51岁女性。磁共振成像显示脑梗中部急性梗死,伴有独特的“米老鼠耳”征。弥散张量成像和束状图显示相对保存的皮质脊髓束,但未检出皮质球束。磁共振血管造影显示脑后动脉及椎基底动脉闭塞。椎基底动脉及其分支狭窄或闭塞导致脑灌注不足可导致BCPI。BCPI的预后和临床表现与受累脑梗梗死的范围及是否累及其他脑区有关。孤立性BCPI可能表现为严重的假性球性麻痹,根据受累模式,肢体功能相对保留。
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Isolated Bilateral Cerebral Peduncular Infarction Manifesting Pseudobulbar Palsy and Quadriparesis: a Case Report.

Bilateral cerebral peduncular infarction (BCPI) is a very rare disorder among stroke patients. The main clinical manifestations in the previously reported BCPI case reports was associated with locked-in syndrome or persistent vegetative state. Here, we present a 51-year-old woman who had pseudobulbar palsy and quadriplegia. Magnetic resonance imaging showed an acute infarction in the middle areas of the cerebral peduncle with a unique "Mickey Mouse ears" sign. Diffusion tensor imaging and tractography showed relatively preserved corticospinal tracts, but the corticobulbar tracts were not detected. Magnetic resonance angiography showed posterior cerebral artery and vertebrobasilar artery occlusion. Cerebral perfusion insufficiency due to stenosis or occlusion of the vertebrobasilar artery and its branches may lead to BCPI. The prognosis and clinical manifestations of BCPI are related to the extent of the infarction in the involved cerebral peduncle and whether other territories are involved. Isolated BCPI may present a severe pseudobulbar palsy with relatively preserved limb function depending on the involvement pattern.

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