240 A case of fulminant guillain-barré syndrome mimicking brain death

暴发型 格林-巴利综合征 医学 儿科 内科学
作者
Jananee Sivagnanasundaram,Rebecca Broad,Lucy Tague,Catarina Quaresma,Richard Dittrich,Fadi Alkufri,Sreedharan Harikrishnan
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:90 (12): e59.1-e59 被引量:1
标识
DOI:10.1136/jnnp-2019-abn-2.198
摘要

Guillain-Barré syndrome (GBS) encompasses a spectrum of acute immune-mediated polyneuropathies. Rarely, in its fulminant form, it can rapidly progress to mimic brain death. We present a case with diagnostic challenges due to a limited history. A 58-year-old gentleman presented generally unwell and within hours of admission choked on his dinner and suffered a cardiorespiratory arrest. Review on ITU revealed absent brainstem reflexes apart from a weak pupillary light response. EEG showed slowing with subtle reactivity, MRI Brain was normal, and CSF revealed albuminocytological dissociation. On day 27 of admission, he was found to follow commands with eye movements, appearing to be in an incomplete locked-in state. Nerve conduction studies confirmed a severe axonal sensorimotor neuropathy with sural sparing. He was treated with plasma exchange and intravenous immunoglobulins and continues to make significant motor improvements each week. This case highlights the crucial recognition of this extreme presentation of GBS, as a misdiagnosis of brain death may lead to the withdrawal of ventilatory support. In a third of reported similar cases there has been a good recovery and in the majority (as in our case) serum ganglioside antibodies have been negative, raising the possibility of alternative nodal and paranodal target antigens.

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