格林-巴综合征和急性播散性脑脊髓炎共病。

IF 1.3
Neurosciences (Riyadh, Saudi Arabia) Pub Date : 2013-04-01
Reema R Mohammed, Mohammed M Jan
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引用次数: 0

摘要

格林-巴勒综合征(GBS)和急性播散性脑脊髓炎(ADEM)是临床上不同的脱髓鞘疾病,它们具有自身免疫发病机制和病毒感染或疫苗接种史。GBS和ADEM同时发生并不常见,报道病例很少。我们的病人是一个10岁的女孩,她表现为急性四肢麻痹,反射性松弛和尿潴留。腰椎穿刺显示轻度细胞增多和蛋白升高。她需要机械通气,静脉注射免疫球蛋白后没有好转。她随后出现了双重视力和意识紊乱。脑MRI显示多发性白质病变提示ADEM。基于时间关联和排除其他病因,我们诊断为GBS和ADEM。经静脉注射甲基强的松龙后,病情明显好转。我们的结论是,GBS和ADEM合并症是一种罕见的实体,表现为严重的神经系统疾病。及时识别和治疗可以加速恢复,从而改善神经系统预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-morbid Guillain-Barré syndrome and acute disseminated encephalomyelitis.

Guillain-Barré syndrome (GBS) and acute disseminated encephalomyelitis (ADEM) are clinically distinct demyelinating disorders that share an autoimmune pathogenesis and prior history of viral infection or vaccination. Concurrent GBS and ADEM are uncommon with few reported cases. Our patient is a 10-year-old girl who presented with acute quadriparesis, areflexia, and urinary retention. Lumber puncture revealed mild pleocytosis and elevated protein. She required mechanical ventilation and failed to improve after intravenous immunoglobulins. She subsequently developed double vision and disturbed level of consciousness. Brain MRI revealed multiple white matter lesions suggestive of ADEM. Based on the temporal association and exclusion of alternative etiologies, we made a diagnosis of GBS and ADEM. She improved remarkably after intravenous methylprednisolone. We conclude that co-morbid GBS and ADEM is an uncommon entity presenting with severe neurological morbidity. Prompt recognition and treatment can hasten the recovery and therefore improve the neurological outcome.

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