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首页> 外文期刊>Journal of the Medical Association of Thailand =: Chotmaihet thangphaet >Acute motor axonal neuropathy with hyperreflexia in a child: A case report
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Acute motor axonal neuropathy with hyperreflexia in a child: A case report

机译：急性运动轴突神经病变与儿童过度重症症：案例报告

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? 2017, Medical Association of Thailand. All rights reserved. ? 2017, Medical Association of Thailand. All rights reserved. Acute motor axonal neuropathy (AMAN), a variant of Guillain-Barré syndrome (GBS), is characterized with acute paralysis and loss of reflexes. This was a case report of AMAN patient presenting with paraparesis and hyperreflexia. We reported a 1-year-11-month-old boy hospitalized with history of two weeks of progressive ascending paralysis. He had upper respiratory tract infection four weeks prior to the onset of weakness. Physical examination showed paraparesis with exaggerated tendon reflexes; furthermore, he was evaluated for spinal cord lesion, which showed normal MRI spine. Lumbar puncture showed CSF cytoalbuminologic dissociation. Moreover, nerve conduction studies showed motor axonal degeneration. His clinical signs improved spontaneously and complete recovery at eight weeks after the onset of weakness. This case implied the clinicians’ extra attention for GBS with hyperreflexia and paraparesis. Acute motor axonal neuropathy (AMAN), a variant of Guillain-Barré syndrome (GBS), is characterized with acute paralysis and loss of reflexes. This was a case report of AMAN patient presenting with paraparesis and hyperreflexia. We reported a 1-year-11-month-old boy hospitalized with history of two weeks of progressive ascending paralysis. He had upper respiratory tract infection four weeks prior to the onset of weakness. Physical examination showed paraparesis with exaggerated tendon reflexes; furthermore, he was evaluated for spinal cord lesion, which showed normal MRI spine. Lumbar puncture showed CSF cytoalbuminologic dissociation. Moreover, nerve conduction studies showed motor axonal degeneration. His clinical signs improved spontaneously and complete recovery at eight weeks after the onset of weakness. This case implied the clinicians’ extra attention for GBS with hyperreflexia and paraparesis.
机译：还2017年，泰国医学协会。版权所有。还2017年，泰国医学协会。版权所有。急性运动轴突神经病变（Aman）是一种突厥 - 巴雷综合征（GBS）的变种，其特征在于急性瘫痪和反射丧失。这是Aman患者呈现术治疗术和超折叠的病例报告。我们报告了一名1年11个月大的男孩住院，历史为期两周的渐进式上升瘫痪。他在弱点前四周进行上呼吸道感染。体检显示夸张的肌腱反射的病原体;此外，他评估了脊髓病变，显示出正常的MRI脊柱。腰椎穿刺表现出CSF细胞增生表现解离。此外，神经传导研究显示了电动机轴突变性。他的临床迹象在弱点发作后八周的八周内自发地改善并完全恢复。这种情况暗示临床医生对Hyperroflex和Paraparesis的GBS额外关注。急性运动轴突神经病变（Aman）是一种突厥 - 巴雷综合征（GBS）的变种，其特征在于急性瘫痪和反射丧失。这是Aman患者呈现术治疗术和超折叠的病例报告。我们报告了一名1年11个月大的男孩住院，历史为期两周的渐进式上升瘫痪。他在弱点前四周进行上呼吸道感染。体检显示夸张的肌腱反射的病原体;此外，他评估了脊髓病变，显示出正常的MRI脊柱。腰椎穿刺表现出CSF细胞增生表现解离。此外，神经传导研究显示了电动机轴突变性。他的临床迹象在弱点发作后八周的八周内自发地改善并完全恢复。这种情况暗示临床医生对Hyperroflex和Paraparesis的GBS额外关注。

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