一名学龄儿童感染腺病毒后出现急性脑炎伴弛缓性麻痹,表现为格林巴利综合征的罕见变异型

R. Loni, Aysha Mohammed Alsindi, Amina Ali Alfaw, G. Fox, Ittrat Abbas, Imlelda Mary Lambert, Bryan Lynch
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引用次数: 0

摘要

格林-巴利综合征(Guillain-Barre syndrome,GBS)、米勒-费舍尔综合征(Miller-Fisher syndrome,MFS)和比克斯塔夫脑干脑炎(Bickerstaff's brainstem encephalitis,BBE)是一系列感染后炎症性免疫介导疾病的综合征。它们可能具有共同的自身免疫致病机制,表现为进行性上升性乏力或弛缓性瘫痪,同时影响儿童和成人。MFS 和 BBE 是 GBS 的罕见变异型,在出现相关特征时应作为鉴别诊断的一部分。我们报告了一例 6 岁男孩的病例,他在腺病毒上呼吸道感染并伴有渗出性扁桃体炎和腹泻后出现咽痛,病程一天,伴有吞咽困难、流涎和口水增多、无法说话或吞咽。临床评估显示,咽反射和咳嗽反射微弱,反射亢进但无阵挛、巴宾斯基反射上行和肌张力低下。根据反射亢进和嗜睡的特殊神经系统表现、血清学研究和核磁共振成像结果,确诊为 BBE。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute encephalitis with flaccid paralysis following an adenoviral infection presenting as a rare variant of Guillain Barre syndrome in a school-age child
Guillain-Barre syndrome (GBS), Miller-Fisher syndrome (MFS), and Bickerstaff’s brainstem encephalitis (BBE) are syndromes which represent a spectrum of post-infectious inflammatory immune-mediated diseases. They may share a common autoimmune pathogenetic mechanism presenting with progressive ascending weakness or flaccid paralysis affecting both pediatric as well as adult populations. MFS and BBE are rare variants of GBS that should be part of the differential diagnosis when relevant features are present. We present a case of a 6-year-old boy, presenting with a sore throat of one-day duration, associated with difficulty in swallowing, increased salivation and drooling, inability to speak or swallow following an adenoviral upper respiratory infection with exudative tonsillitis and diarrhea. Clinical evaluation showed weak gag reflex and cough reflex, hyperreflexia without clonus, upgoing Babinski reflexes, and hypotonia. A diagnosis of BBE was made based on specific neurological manifestations of hyperreflexia and drowsiness, serological studies, and MRI findings.
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